Stability Testing of Dietary Supplements: Assessment of Quality and Safety

The stability of dietary supplements is crucial to ensuring their quality and safety. Stability testing is a comprehensive process that allows the assessment of how storage conditions affect the composition of supplements and their shelf life before they reach the consumer.

The Importance of Stability of Dietary Supplements

Why is stability testing necessary?

Stability testing is essential to ensure that a dietary supplement maintains its health properties throughout its shelf life. Without stability testing, the consumer has no certainty whether the active ingredients in the supplement have degraded.

How does stability affect the quality of supplements?

The stability of dietary supplements directly affects their quality. If a supplement is not stable, physicochemical changes may occur, the content of active ingredients may decrease, and even the development of microorganisms may take place, which threatens the safety of supplements.

Active ingredients and their degradation

Active ingredients in dietary supplements may degrade under the influence of external factors. Stability testing helps determine how humidity, temperature, and light affect the stability of supplements containing sensitive ingredients.

Types of Stability Testing

Long-term testing

Long-term testing is a type of stability testing conducted throughout the declared shelf life of a dietary supplement. The sample is stored under controlled conditions to monitor quality changes.

Accelerated testing

Accelerated testing is an important element in assessing the stability of dietary supplements. In this type of testing, the sample is subjected to extreme conditions, which allows the prediction of long-term stability in a short period.

Climatic conditions in testing

Climatic conditions during stability testing are strictly controlled and adjusted to the climatic zones in which the dietary supplement will be available. This helps ensure that the stability of dietary supplements is adequate for storage conditions.

Conducting Stability Testing

Controlled laboratory conditions

Stability testing of dietary supplements must be conducted under controlled laboratory conditions, in accordance with GMP principles. Only in this way can the reliability and reproducibility of dietary supplement testing be ensured.

Monitoring physicochemical parameters

During stability testing of dietary supplements, it is necessary to monitor physicochemical parameters. This allows the detection of any changes in the composition of the supplement that may affect its quality and safety.

Microbiological analysis of products

Microbiological analysis is a key element in the assessment of dietary supplement stability. We examine whether microorganisms develop in the product that could pose a threat to consumer health and reduce the quality of dietary supplements.

Test Results and Their Interpretation

Determining the minimum stability date

The results of storage testing form the basis for determining the minimum stability date of a dietary supplement. This date informs the consumer until when the supplement maintains full effectiveness and safety.

The importance of labeling and packaging of dietary supplements

The label on a dietary supplement should include information about storage conditions and the minimum durability date. Supplement packaging is intended to protect the product from external factors that may affect its stability.

Examples of dietary supplement testing

As part of dietary supplement testing, the stability of vitamins, minerals, probiotics, and other active ingredients is assessed. The scope of testing includes composition analysis, evaluation of physicochemical and microbiological parameters to ensure the safety of dietary supplements.


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Determination of the TOTOX Index in Dietary Supplements – The Importance of the Oxidation Indicator in Assessing the Quality of Omega-3 Oils

The winter period is conducive to reviewing quality processes and verifying product stability. In the case of dietary supplements containing oils—particularly omega-3 fatty acids derived from fish and algae—their susceptibility to oxidation remains a key issue. One of the most comprehensive parameters for assessing this process is the TOTOX (Total Oxidation Value) index, which serves as an essential quality control tool for lipid-based supplements.

Introduction to the TOTOX Index

An introduction to the TOTOX index is essential for understanding how oil quality is assessed in dietary supplements, especially those rich in omega-3 fatty acids. Omega-3 supplementation is popular due to its numerous health benefits; however, oxidation of the contained fats may negatively affect their efficacy.

What Is the TOTOX Index?

The TOTOX index is a parameter used to determine the degree of oxidation of fats, such as omega-3 fatty acids, in dietary supplements. The name TOTOX stands for Total Oxidation Value. The TOTOX value takes into account both primary and secondary oxidation products.

The Importance of Freshness in Omega-3 Supplements

Freshness is a critical factor in omega-3 supplements. The freshness of the oil directly translates into its quality and effectiveness. A low TOTOX value indicates high-quality fish oil and, consequently, better bioavailability of omega-3 fatty acids. A supplement characterized by a lower TOTOX value will demonstrate superior performance characteristics.

The Oxidation Process of Omega-3 Oils

Oxidation of omega-3 oils is an inevitable process that affects supplement quality. Understanding the mechanisms behind this process is crucial for dietary supplement manufacturers, as it enables the implementation of appropriate strategies to minimize the negative impact of fat oxidation on omega-3 fatty acids and maintain high product quality.

Causes of Fish Oil Oxidation

There are numerous causes of fish oil oxidation. Due to its high content of polyunsaturated fatty acids, fish oil is highly susceptible to external factors such as oxygen, light, and temperature. Improper storage of dietary supplements—for example, under unsuitable conditions—accelerates the oxidation process.

Effects of Oxidation on Supplement Quality

The effects of oxidation on supplement quality are multifaceted. First and foremost, oxidation leads to the formation of undesirable substances such as peroxides and aldehydes, which may be harmful to health. Additionally, this process reduces product freshness and alters its taste and odor, affecting consumer acceptance.

How to Monitor the Level of Oxidation?

Regular laboratory testing is essential. Measurement of the TOTOX value allows ongoing control of the oil’s oxidation level and enables corrective action if oxidation exceeds permissible limits. Moreover, it is important to monitor the TOTOX index at various stages of dietary supplement production.

Analysis of the TOTOX Index

Analysis of the TOTOX index enables a comprehensive assessment of oil quality in dietary supplements by providing information about the current state of oxidation. Understanding the components of this index—such as the Peroxide Value (PV) and the Anisidine Value (AV)—is crucial for interpreting results and making appropriate decisions regarding supplement quality.

The Role of the Peroxide Value (PV) in Quality Assessment

The Peroxide Value (PV) plays a key role in quality assessment because it indicates the content of primary oxidation products, namely peroxides. A high PV may suggest that the fat oxidation process has recently begun. Measurement of PV is particularly important in evaluating fish oil quality.

TOTOX and the Quality of Omega-3 Supplements

Benefits of Regular TOTOX Testing

Regular testing of the TOTOX index in dietary supplements containing omega-3 fatty acids provides measurable benefits. It allows verification that oils, including fish oil, maintain high quality throughout their shelf life. As a result, manufacturers can ensure that supplementation is both safe and effective, and that omega-3 fatty acids retain their functional properties.

Impact on Technological Processes

Monitoring the TOTOX value significantly influences technological processes. It enables manufacturers to optimize oil production processes, including fish oil processing, through the appropriate selection of antioxidants—such as vitamin E—and suitable storage conditions. This helps minimize fat oxidation and maintain a low TOTOX value.

Transparency and Consumer Trust

Regular TOTOX testing enhances transparency and builds consumer trust. Information about a low TOTOX value, indicating fresh fish oil, can form part of the marketing communication of an omega-3 supplement. When consumers see confirmation of high quality, they are more likely to purchase the product.

Best Practices in Quality Control

Good Practices in Oil Quality Assessment

Best practices in assessing oil quality, including fish oils, involve regular monitoring of the TOTOX index. It is important that analyses are performed in accordance with recognized standards to ensure result reliability. Additionally, TOTOX values should be included in oil specifications.

Quality Assurance Systems and TOTOX

The TOTOX value constitutes an integral part of quality assurance systems in the production of omega-3 dietary supplements. Monitoring the degree of fat oxidation allows continuous control of the production process and rapid response if permissible limits are exceeded, thereby ensuring high final product quality.

The Role of TOTOX in Meeting Quality Standards

The role of TOTOX in meeting quality standards is crucial. Many organizations, such as the Global Organization for EPA and DHA (GOED), establish limits for TOTOX values in fish oils. Compliance with these standards confirms that an omega-3 supplement is safe and effective, and that its EPA and DHA content is consistent with the declared values.

TOTOX Testing in J.S. Hamilton Laboratories

Scope of Analytical Services

J.S. Hamilton laboratories offer a wide range of analytical services for determining the TOTOX index in dietary supplements containing oils, including fish oil. We provide comprehensive analysis covering both Peroxide Value (PV) and Anisidine Value (AV) measurements, enabling precise assessment of fat oxidation.

Analytical Methods Used in Testing

In our testing, we apply advanced analytical methods that ensure precise and reliable TOTOX measurements. We use spectrophotometric techniques that allow accurate determination of peroxide content and secondary oxidation products in oils, including fish oil.

Support for Dietary Supplement Manufacturers

As an accredited laboratory, we support dietary supplement manufacturers in monitoring the quality of their products. We assist in interpreting TOTOX test results and provide guidance on optimizing production processes to ensure the stability and freshness of omega-3 fatty acids in supplements.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Trends in the cosmetics research industry in February – effectiveness and new equipment possibilities

Winter months do not slow down development processes in the cosmetics industry. On the contrary, this period is often dedicated to structuring documentation, verifying regulatory requirements and planning studies that form the foundation for safe and credible product launches. The February overview covers both key research directions and practical solutions supporting objective efficacy assessment.

COSMETOTEST 2026 – AN INTERNATIONAL PLATFORM FOR SCIENTIFIC EXCHANGE

On 18–19 March 2026, Cosmetotest 2026 will take place in Lyon and online. This international symposium is dedicated to preclinical and clinical testing in cosmetology and brings together R&D experts, scientists, research laboratories and instrumentation providers.

This year’s edition focuses on four major scientific areas:

  • the influence of hormones on skin and hair,
  • the role of the exposome in ageing processes,
  • advanced methodologies for hydration assessment,
  • the skin–brain axis as an emerging research direction.

These topics reflect the growing importance of interdisciplinary approaches combining dermatology, biochemistry, neurobiology and advanced instrumental analysis. For laboratories, this translates into the continuous development and validation of innovative efficacy assessment methods.

COSMETICBUSINESS 2025 – MARKET TRENDS AND THEIR IMPACT ON TESTING METHODOLOGIES

During CosmeticBusiness 2025 in Munich, more than 400 exhibitors from 29 countries presented innovations under the slogan “Where Beauty Starts”. Clean beauty concepts and sustainability were at the forefront of discussions.

Key trends included:

  • plant-based and biotechnological ingredients,
  • environmentally responsible production processes,
  • reduction of plastic usage,
  • refill systems and recyclable packaging solutions,
  • circular economy strategies.

The rapid evolution of formulations, including powder-based cleansing products, algae-derived actives, bioengineered extracts and innovative elastin technologies, requires equally advanced and reliable testing methodologies. As product concepts evolve, laboratories must adapt their instrumental techniques and standardised protocols to ensure credible and reproducible results.

BIOREVITALISATION EFFECT – HOW TO SUBSTANTIATE A COMPLEX CLAIM?

“Biorevitalisation” is a multidimensional claim encompassing improvements in firmness, elasticity, hydration and overall skin condition. From a research perspective, such a claim requires a comprehensive and complementary measurement strategy.

A dedicated efficacy testing package for the biorevitalisation effect may include:

  • volumetric and filling assessments,
  • hydration level measurements,
  • transepidermal water loss (TEWL) analysis,
  • additional parameters supporting skin barrier evaluation.

An integrated testing approach enables a coherent interpretation of product performance and provides robust quantitative data to support marketing communication and product documentation.

IN VIVO HYDRATION ASSESSMENT – METHODOLOGY AND INSTRUMENTATION

In vivo evaluation of skin hydration is primarily based on the analysis of electrical properties of the skin and the measurement of water loss through the epidermis. Studies are conducted under strictly controlled environmental conditions, including defined humidity and temperature, standardised product dosage, a specified test area (typically the volar forearm) and placebo control.

Different instruments are used depending on the depth of measurement:

  • Stratum corneum – Corneometer®, Dermalab, Epsilon (Biox), MoistureMeter SC, Skicon-200, DPM 9003,
  • Epidermis – MoistureMeterEpiD,
  • Dermis – MoistureMeterD.

A second widely recognised method involves indirect hydration assessment through TEWL measurement using the Tewameter TM 300. This method is particularly relevant for oil-based formulations, which may interfere with impedance-based measurements, and provides valuable information regarding overall skin barrier function.

The precise selection of measurement techniques in relation to product type and declared claim is essential to ensure repeatable and scientifically sound outcomes.

PRIMOS CR 45 – THREE-DIMENSIONAL SKIN TOPOGRAPHY ANALYSIS

The implementation of PRIMOS CR 45 technology enables advanced volumetric and structural skin assessments. This system is based on three-dimensional topography analysis and delivers both quantitative numerical data and high-resolution visual documentation of changes before and after product application.

The technology is particularly suitable for:

  • lip volume enhancement evaluation,
  • assessment of under-eye puffiness reduction,
  • surface smoothing and wrinkle analysis.

Objective, reproducible measurements supported by visual evidence significantly strengthen efficacy documentation and provide a reliable basis for substantiating product claims.


The cosmetics industry is moving towards increasingly complex formulations, multidimensional marketing claims and heightened expectations regarding data transparency. Addressing these challenges requires the integration of advanced testing methodologies, precise instrumental analysis and standardised in vivo protocols.

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Verify the Active Compounds Content in Your Dietary Supplements: An Essential Verification Program

In the competitive dietary supplements market, ensuring the quality and safety of your products is paramount. Precise verification of active compounds is not just a regulatory requirement but a cornerstone of consumer trust. This article explores the critical aspects of a dietary supplement verification program, highlighting the importance of accurate testing and compliance with industry standards.

Importance of Dietary Supplement Verification

The dietary supplements industry faces increasing scrutiny regarding the accuracy of product labels and the actual content of active ingredients. Independent audits and laboratory testing are essential to confirm that supplement products meet the stated claims and comply with both national and international regulations. Regular testing safeguards consumer health and enhances brand credibility within the dietary supplements market.

Understanding the Dietary Supplement Label

The dietary supplement label serves as the primary source of information for consumers. It must accurately reflect the identity and quantity of active ingredients, dosage recommendations, and any potential allergens. Ensuring that the supplement label is truthful and compliant with food law requires rigorous testing and verification processes, protecting consumers from misleading or false claims and ensuring food safety.

Role of Active Ingredients in Product Efficacy

Active ingredients determine the efficacy of dietary supplements containing specific compounds. Whether it’s amino acids, vitamins, or herbal extracts, their presence and potency must align with the manufacturer’s declaration. Testing methods like mass spectrometry are crucial for accurately quantifying these biologically active components, ensuring that the supplement’s claimed benefits are substantiated and that the product delivers the intended therapeutic effect.

Regulatory Compliance for Food Supplements

Compliance with regulations, such as those set forth by the European Parliament and of the Council and the U.S. Food and Drug Administration (FDA), is essential for food supplements manufacturers. These regulations encompass various aspects, including good manufacturing practices (GMP), accurate labeling, and the absence of contaminants like heavy metals. Adhering to these standards not only ensures market access but also builds consumer confidence in the safety and quality of dietary supplements.

To ensure the highest standards of quality and compliance for your dietary supplements, partner with J.S. Hamilton laboratories. Our accredited facility offers comprehensive testing services, from single vitamin analyses to complete mineral profiles, ensuring accurate verification of active ingredient content and adherence to regulatory requirements. Contact us today to learn more about our services and how we can support your commitment to product excellence.

Analytical Techniques for Accurate Verification

Mass Spectrometry in Dietary Supplement Testing

Mass spectrometry is a pivotal analytical technique in the verification of substances in dietary supplements. This sophisticated method allows for precise identification and quantification of active ingredients, ensuring that dietary supplements containing these compounds meet the manufacturer’s declaration. By utilizing mass spectrometry, laboratories can detect even trace amounts of biologically active components, thereby confirming the quality of dietary supplements and bolstering consumer confidence.

Advanced Methods for Elemental Composition Analysis

Analyzing the elemental composition of food supplements is crucial to detect heavy metals and other contaminants. Advanced methods, such as inductively coupled plasma mass spectrometry (ICP-MS), offer high sensitivity and accuracy in determining the presence and concentration of various elements. This ensures that substances in dietary supplements meet stringent regulatory standards, preventing potential harm to consumers and maintaining compliance with the U.S. Food and Drug Administration and European Parliament and of the Council guidelines.

HPLC and Its Application in Supplement Verification

High-Performance Liquid Chromatography (HPLC) is widely used in the verification of active compounds within dietary supplements. This technique separates, identifies, and quantifies each component, ensuring the supplement’s potency and purity. HPLC is particularly effective for analyzing amino acids, vitamins, and other active ingredients, thereby supporting the accuracy of the dietary supplement label and affirming compliance with good manufacturing practices.

Benefits of Accurate Testing for Manufacturers

Establishing Credibility Through Accurate Declarations

Accurate testing and verification of active ingredients are essential for establishing credibility in the dietary supplements market. When manufacturers can demonstrate that their product label accurately reflects the content of active compounds, they build trust with consumers. This transparency not only enhances brand reputation but also provides a competitive edge, as consumers increasingly demand detailed information and evidence of product quality and safety of dietary supplements.

Maintaining Product Stability and Safety

Rigorous testing ensures that food supplements maintain their stability and safety throughout their shelf life. Regular analysis helps to detect any degradation of active ingredients, preventing products from falling below the claimed potency. By adhering to good manufacturing practices and conducting thorough audits, manufacturers can ensure that their supplement products remain effective and safe for consumption, compliant with food law and regulatory standards.

Implementing a Dietary Supplement Verification Program

Steps to Develop an Effective Verification Strategy

An effective dietary supplement verification program begins with a comprehensive risk assessment. It’s important to identify potential hazards. These hazards might include elements like:

  • Heavy metals
  • Inaccurate active ingredients

Testing should then be prioritized based on the identified risk. Furthermore, regular audits of good manufacturing practices (GMP) should be incorporated to ensure compliance with standards set by the U.S. Food and Drug Administration and the European Parliament and of the Council. This proactive approach helps maintain the quality of dietary supplements and ensures food safety.

Key Considerations for Quality Assurance Audits

When conducting quality assurance audits, focus on verifying the manufacturer’s adherence to established protocols. Ensure that the dietary supplement label accurately reflects the content of active compounds, including amino acids and vitamins. Verify the accuracy of the declared dosage and confirm the absence of harmful substances in dietary supplements, such as heavy metals. A thorough audit process safeguards the integrity of food supplements and protects consumers in the polish market. Regular audits ensure compliance with food law and good manufacturing practices.

Conclusion and Invitation to Utilize Laboratory Services

In conclusion, a robust dietary supplement verification program is essential for ensuring the quality of dietary supplements, compliance with regulations, and consumer safety. Accurate verification of active ingredients, regular audits, and adherence to good manufacturing practices are critical components of this process. Manufacturers who prioritize these measures can establish credibility, maintain product stability, and gain a competitive edge in the dynamic dietary supplements market. Accurate verification methods like mass spectrometry and HPLC, ensure the product quality of dietary supplements.

Contact Us for Comprehensive Testing Solutions

Ensure the safety and efficacy of your dietary supplements by partnering with J.S. Hamilton laboratories. Our accredited facility offers comprehensive testing services, from single active ingredients analyses to complete mineral profiles, ensuring accurate verification of active compounds and adherence to regulatory requirements. Whether you need to verify the elemental composition or confirm the presence of specific amino acids, our experts provide information and support to meet all your testing needs. Trust J.S. Hamilton to elevate your commitment to quality of dietary supplements and consumer trust. Contact us today to discuss your testing program and how we can help you meet and exceed industry standards.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Assessment of Dietary Supplement Efficacy & Food Effects

In today’s market, the assessment of dietary supplements and food products is crucial for manufacturers aiming to meet consumer expectations and regulatory demands. With the number of dietary supplement options available, instrumental analysis provides a robust method to confirm the efficacy of these products and ensure they deliver on their promises.

Importance of Dietary Supplement Assessment

The assessment of dietary supplements is critical for several reasons, primarily revolving around consumer safety and product efficacy. Thorough analysis ensures that supplements contain the ingredients they claim, in the correct concentrations, and that these ingredients are bioavailable. This protects consumers from potential health risks associated with ineffective or improperly formulated products. The role of instrumental testing cannot be overstated.

Market Growth and Consumer Expectations

The dietary supplement market has experienced a substantial increase in recent years. This growth is driven by consumers seeking to improve their health and well-being through dietary interventions. As a result, consumer expectations regarding the efficacy of dietary supplements are also on the rise. They expect visible and tangible health benefits, placing pressure on manufacturers to deliver high-quality, effective products. This requires careful consideration of product formulation, rigorous testing, and transparent communication of results.

Regulatory Standards and Compliance

Stringent regulatory standards govern the dietary supplement industry to safeguard public health. These regulations mandate that manufacturers provide evidence supporting the safety and efficacy of their products. Compliance with these standards is essential for market access and maintaining consumer trust. The assessment of dietary supplements through instrumental analysis helps manufacturers meet these regulatory requirements by providing documented proof of product quality and consistency. The use of analytical methods ensures that the dietary supplement complies with regulations.

Role of Instrumental Testing in Quality Assurance

Instrumental testing plays a pivotal role in the quality assurance of dietary supplements. It offers precise and reliable methods for identifying and quantifying active ingredients, detecting contaminants, and evaluating product stability. The use of techniques such as HPLC, GC-MS, and ICP-MS provides manufacturers with detailed information about the composition and properties of their supplements. This data is invaluable for ensuring product quality, consistency, and efficacy. Instrumental testing is used in dietary supplements.

If you want to base the effectiveness of your supplement on hard data, not just marketing claims, J.S. Hamilton laboratories will prepare an optimal instrument testing program for you.

Types of Instrumental Analyses for Dietary Supplements

Determination of Active Ingredients

The determination of active ingredients is a critical step in assessing the efficacy of dietary supplements. Instrumental analysis, such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography-Mass Spectrometry (GC-MS), plays a vital role in this process. These sophisticated techniques allow for precise identification and quantification of vitamins, minerals, and other bioactive compounds present in dietary supplements. Accurate assessment ensures that the supplements contain the declared concentration of active ingredients, which directly impacts the health and potential benefits for consumers.

Bioavailability and Release Testing

Bioavailability and release testing are essential for understanding how effectively the body can absorb and utilize the active ingredients in dietary supplements. These tests evaluate the rate and extent to which ingredients are released from the supplement matrix and become available for absorption in the gastrointestinal tract. Dissolution testing, a common method, simulates the conditions found in the stomach and intestines to assess the release profile of active compounds. Proper analysis can significantly improve the dietary supplement’s impact on health.

Stability Analysis of Active Ingredients

Stability analysis is crucial for ensuring that dietary supplements maintain their efficacy and safety throughout their shelf life. Factors such as temperature, humidity, and light exposure can degrade active ingredients, reducing their concentration and potentially forming harmful byproducts. Stability studies involve subjecting supplements to various environmental conditions and periodically analyzing the concentration of active ingredients. This assessment helps manufacturers determine appropriate storage conditions and expiration dates, ensuring consumers receive products of consistent quality.

Authenticity and Purity Assessment

The authenticity and purity assessment of ingredients is vital for guaranteeing the quality and safety of dietary supplements. Instrumental analysis techniques, such as mass spectrometry and isotope analysis, are used to verify the source and purity of raw materials. These methods can detect adulteration, contamination, and the presence of synthetic compounds that may pose health risks. Ensuring the authenticity and purity of ingredients protects consumers from potential harm and reinforces confidence in the dietary supplement.

If you want to base the effectiveness of your supplement on hard data, not just marketing claims, J.S. Hamilton laboratories will prepare an optimal instrument testing program for you.

Benefits of Instrumental Testing for Manufacturers

  • Enhancing Brand Credibility
  • Facilitating Market Entry and Regulatory Compliance
  • Risk Mitigation and Quality Control

Conclusion: The Value of Reliable Assessment

Building Trust Through Data-Driven Evidence

Building trust in the dietary supplement industry requires moving beyond marketing claims and providing data-driven evidence. The assessment of dietary supplements through instrumental analysis offers a reliable and transparent way to demonstrate the efficacy, safety, and consistency of products. By embracing these methods, manufacturers can foster greater confidence among consumers and healthcare professionals, and dietary supplement use will gain greater trust.

Invitation to Utilize Our Laboratory Services

J.S. Hamilton laboratories provide comprehensive instrumental testing services tailored to meet the unique needs of dietary supplement manufacturers. Our experienced team utilizes state-of-the-art equipment and validated methodologies to deliver accurate, reliable results. Whether you require analysis of active ingredients, bioavailability testing, stability studies, or authenticity assessment, we offer solutions to support your quality assurance and regulatory compliance efforts, to ensure the assessment of dietary supplements.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Doping Testing in Nutritional Products and Dietary Supplements

Doping in sport is a problem that affects both amateur and professional athletes. In the context of dietary supplements and sports nutrition products, doping testing becomes crucial for protecting athletes’ health and maintaining fair competition. This article discusses doping-related aspects of supportive products, highlighting potential risks and the need for proper control.

What Is Doping in Sport?

Doping in sport is defined as the use of prohibited substances or prohibited methods to enhance an athlete’s physical or mental performance. The doping issue is often linked to nutritional products and dietary supplements, which may contain banned substances even if they are not declared on the label. Supplement testing is therefore essential to protect athletes from inadvertent doping and positive anti-doping test results.

Definition and Objectives of Doping

Doping includes the use of prohibited substances and methods to gain a competitive advantage in sport. The objective is often rapid muscle mass increase or performance enhancement, which violates sports ethics and fair play principles. Athletes who use banned substances risk disqualification and serious health consequences. The World Anti-Doping Agency (WADA) regularly publishes the List of Prohibited Substances and Methods.

Impact of Doping on Athletes

Doping has a negative impact on athletes’ health and may lead to serious disorders. The most common consequences include:

  • heart and liver damage
  • hormonal disorders

The use of prohibited substances may also lead to addiction and mental health problems. The consequences of doping can be long-term and irreversible. This is why anti-doping control and supplement testing are so important for protecting athletes from harmful effects.

Sports Ethics and Doping

Sports ethics is the foundation of fair competition, and doping constitutes a serious violation of it. The use of prohibited substances undermines fair play and public trust in sport. Anti-doping efforts are essential to protect the integrity of sport and ensure equal opportunities for all athletes. Consumers should be aware of the risks associated with nutritional products and dietary supplements that may contaminate the body with banned compounds.

Dietary Supplements and the Risk of Doping

Risk of Supplement Contamination

The risk of dietary supplement contamination is a real threat for athletes. Products available on the supplement market may contain banned substances that are not declared on the label. These prohibited compounds may result from cross-contamination during manufacturing or from the intentional addition of doping agents by producers. As a result, an athlete may unknowingly consume banned substances, which can lead to positive anti-doping test results and disqualification.

How to Avoid Inadvertent Doping

To avoid inadvertent doping, athletes should exercise particular caution when selecting dietary supplements. It is essential to use products from reputable manufacturers who subject their nutritional products and supplements to rigorous testing. Labels should be reviewed carefully and quality certifications confirming the absence of prohibited substances should be verified. Consultation with a sports dietitian can help in selecting safe supplements and minimizing the risk of violating anti-doping regulations.

The Role of Labeling in Supplementation

Labeling plays a key role in supplementation. It provides information about the composition of the dietary supplement, including a list of active ingredients. Athletes should carefully analyze labels for substances included on the WADA Prohibited List. It should be noted that not all doping agents are always clearly declared, which further emphasizes the importance of choosing certified products that have undergone supplement testing.

Anti-Doping Testing of Dietary Supplements

Why Commission Testing?

Commissioning anti-doping testing of dietary supplements is crucial for ensuring safety and fairness in sport. Such testing makes it possible to detect prohibited substances that may contaminate a supplement, even if they are not listed on the label. Supplement testing protects athletes from inadvertent doping and positive anti-doping results. Regular anti-doping control of supplements helps maintain high quality and safety standards on the supplement market.

J.S. Hamilton Laboratories and Their Role in Quality Control

Laboratories such as J.S. Hamilton play an important role in dietary supplement quality control. They conduct supplement testing for the presence of prohibited substances, providing athletes and manufacturers with assurance that products are free from banned compounds. Through precise analytical testing, laboratories support anti-doping efforts and protect athlete health. Testing performed by an accredited laboratory can confirm that a given supplement complies with anti-doping regulations.

Examples of Anti-Doping Tests

Examples of anti-doping tests include the analysis of nutritional products and dietary supplements for anabolic steroids, hormones, stimulants, and other substances listed on the WADA Prohibited List. Testing methods can detect even trace amounts of banned substances that may have entered a product during manufacturing. Test results are confidential and provided to the client, enabling appropriate actions to ensure product safety and athlete protection.

Most Common Doping Substances

Anabolic Steroids

Anabolic steroids are prohibited substances that mimic the effects of testosterone, the hormone responsible for muscle development. Athletes sometimes use these banned substances to rapidly increase strength and muscle mass. However, anabolic steroids are associated with serious side effects, including:

  • cardiovascular and liver disorders,
  • hormonal imbalance.

Supplement testing frequently detects prohibited substances, which may lead to athlete disqualification and fair play violations.

Hormones and Growth Factors

Hormones and growth factors represent another group of prohibited substances in sport. Erythropoietin (EPO) increases red blood cell production, improving oxygen capacity. Growth hormone affects metabolism and tissue regeneration. Abuse of these substances is associated with serious health risks, including heart disease and cancer. Anti-doping control aims to detect these compounds to protect athlete health and competition integrity.

Beta-2 Agonists and Stimulants

Beta-2 agonists dilate the bronchi, facilitating breathing and potentially improving endurance performance. Other substances also affect athlete performance, including stimulants such as amphetamines, which activate the nervous system, reduce fatigue, and increase focus. Some of these compounds may be present in dietary supplements and are a common cause of positive anti-doping test results. Stimulant abuse may lead to addiction, cardiac arrhythmias, and stroke. Athletes should be aware of the risks associated with these prohibited substances.

Doping Testing at J.S. Hamilton

The Importance of Informed Supplementation in Sport

Informed supplementation is essential to avoid inadvertent doping. Athletes should carefully review supplement and nutrition product labels to ensure the absence of prohibited substances. Consultation with a sports dietitian supports safe product selection. Independent laboratory testing of supplements provides confirmation that products are free from banned compounds and reduces the risk of positive anti-doping results.

Protecting Athlete Health Against Doping

Protecting athlete health from doping is a priority in sport. The use of prohibited substances carries serious short- and long-term health consequences. Anti-doping control and supplement testing help detect and eliminate banned substances from the market. Education on doping-related risks is necessary so that athletes can make informed and responsible decisions.

Shared Responsibility in the Fight Against Doping

The fight against doping requires shared responsibility among all stakeholders in sport, including athletes, coaches, supplement manufacturers, and sports organizations. Manufacturers should ensure product quality and purity through rigorous testing. Sports organizations should implement effective anti-doping programs, educate athletes, and enforce compliance. Scientific research plays a key role in identifying new doping agents and developing effective detection methods.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

New Update in FCM: Regulation (EU) 2026/245 is here!

The landscape of Food Contact Materials (FCM) in the EU continues to evolve, and the recent publication of Commission Regulation (EU) 2026/245 (amending Annex I of 10/2011) marks another critical step for the industry. 

If you are used to seeing the “Restrictions and Specifications” column in Annex I as mostly empty, it’s time to look again. This update demonstrates a clear trend: that last column is filling up with complex requirements that are now vital for compliance. 

The “Empty Column” is Filling Up 

The new amendment introduces substances where a standard migration limit (SML) isn’t the only hurdle. We are seeing a significant shift toward use limits (composition limits). 

Instead of just testing the final “leakage,” we now have limits such as max 0.1% w/w in the final polymer. 

This means compliance can no longer be verified by testing alone; it relies on precise data sharing within the supply chain. 

Connection to EU 2025/351 & Purity Criteria 

This isn’t just a list of new substances; it is the practical application of the standards set by EU 2025/351. The “Quality Amendment” era has turned these principles into mandatory requirements: 

Purity Standards: New substances must meet strict purity criteria. If your Declaration of Compliance (DoC) doesn’t reflect this verification, the material is technically non-compliant. 

Information Flow: The DoC is no longer a static document but a critical link for transferring compositional data that the next producer cannot find out through testing. 

Article 14a: When Restrictions Meet the Label 

Under the new Article 14a (Labelling) requirements, the restrictions in that “last column” must now be clearly communicated to the end-user when safety depends on it. Examples from the new amendment include: 

Food Type Restrictions: “Restricted to contact with non-fatty foods only.” 

Sensitive Groups: “Not authorized for infant formula or human milk.” 

These are no longer just technical notes – they are mandatory labeling elements that must be visible and clear to prevent misuse. 

 Why this matters for your Supply Chain 

The combination of EU 2026/245 and EU 2025/351 means that a generic “complies with 10/2011” statement is essentially obsolete. To be compliant, your DoC must now be the “Source of Truth” for: 

  • Purity verification of new substances. 
  • Specific Use Limits (w/w) for converters. 
  • Clear instructions for the final labeling of the product. 

The “last column” is now the most important one. How is your team ensuring this data flows correctly from your suppliers? Let’s discuss below! 


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Storage testing of dietary supplements – check how long your product retains its value in various climate zones

The stability of dietary supplements is one of the key elements of their quality. Consumers expect that the declared content of active ingredients will be maintained throughout the shelf life and that the product will be safe and comply with the specifications. To guarantee this, manufacturers use stability studies to assess how a supplement behaves over time, in different climatic conditions and at different temperatures and humidity levels.

At J.S. Hamilton laboratories, we support companies in implementing comprehensive stability testing programs that comply with international guidelines and market requirements.

Why is it worth conducting stability studies?

The active ingredients in supplements — vitamins, minerals, plant extracts, probiotics, fatty acids, and enzymes — can degrade as a result of:

  • temperature,
  • humidity,
  • exposure to light,
  • oxidation,
  • interactions between ingredients.

The lack of stability testing can lead to:

  • loss of potency of active ingredients,
  • changes in color, smell, texture,
  • delamination of capsules or tablets,
  • reduced microbiological safety,
  • risk of complaints and batch recalls.

Storage studies in different climate zones

The world has been divided into climate zones according to ICH guidelines. Supplements sold globally should be evaluated under conditions representative of specific regions:

Zone I – temperate climate (e.g., Northern Europe)

Long-term conditions: approx. 21°C / 45–55% RH Application: most products sold in the EU.

Zone II – subtropical and Mediterranean climate (e.g., Southern Europe)

Long-term conditions: 25°C / 60% RH Risk: accelerated degradation of vitamins and extracts.

Zone III – hot and dry climate

Long-term conditions: 30°C / 35% RH Risk: intense drying and oxidation of ingredients.

Zone IV – hot and humid climate (South Asia, Latin America)

Long-term conditions: 30°C / 65–75% RH Greatest risk: degradation of active ingredients, growth of microorganisms, destabilization of soft and hard capsules.

How are stability studies conducted at J.S. Hamilton?

We offer both long-term and accelerated stability studies, performed in accordance with current guidelines.

  1. Study design
  • Analysis of the formulation and form (tablets, capsules, sachets, liquids, oils)
  • selection of appropriate climate zones,
  • determination of the range of parameters to be monitored.
  1. Storage in climate chambers

Controlled temperature and humidity, in accordance with ICH standards.

  1. Periodic analyses

We test, among other things:

  • active ingredient content (vitamins, minerals, extracts),
  • physicochemical parameters,
  • microbiological stability,
  • organoleptic characteristics,
  • the performance of capsules and tablets in disintegration tests.
  1. Final report

The manufacturer receives full information about the shelf life of the product, its behavior over time, and recommendations regarding packaging and the declared expiration date.

What does the manufacturer gain?

  • Confidence that the declared content of ingredients is maintained,
  • Safe shelf life,
  • Proof of compliance with EU and foreign market requirements,
  • Support with product registration and audits,
  • Reduced risk of complaints and financial losses.

Storage tests are an essential part of quality control for dietary supplements. They allow you to determine how long a product remains stable and safe — both on the European market and in various, more demanding climatic zones.

If your supplement is to be launched on the international market or you need to confirm its shelf life, J.S. Hamilton laboratories will prepare a complete stability testing program for you — tailored to the formulation, product type, and target market.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

New Year in the cosmetology laboratory – Regulations, Events, and Practical Information for the Start of the Year

The beginning of the year is a good time to organize the most important information for the cosmetics industry and to look ahead to the coming months from the perspective of regulatory changes, planned events, and practical aspects of laboratory cooperation. In the latest edition of COSM updates, we summarize key topics that may be relevant for cosmetics manufacturers and distributors in the first half of the year.

FASTER TEST IMPLEMENTATION THANKS TO IMPROVEMENTS IN THE CLIENT PORTAL

One of the factors that has a real impact on the pace of research project execution is the completeness of documentation at the order submission stage. Adding all required attachments directly in the Client Portal enables smoother information flow between teams and reduces the risk of formal deficiencies.

In practice, this means a faster start of testing, more efficient sample analysis, and shorter turnaround times for the final report—particularly important for projects carried out under market-driven time pressure.

INDUSTRY ACTIVITY AND INTERNATIONAL DEVELOPMENT

In recent months, we have participated in key industry trade fairs and conferences, including events in Amsterdam, Munich, Berlin, Barcelona, and Valencia, as well as domestic events dedicated to the cosmetics industry and aesthetic medicine. These meetings have allowed us not only to strengthen our brand position but also to initiate new projects and collaborations.

At the same time, we have been conducting intensive commercial activities, particularly in Southern European markets and beyond Europe. Numerous meetings with partners and clients have resulted in relationships that are currently entering the implementation and project development phase.

INDUSTRY EVENT CALENDAR – WHERE TO MEET US IN 2026

The coming months will also bring further opportunities for direct industry meetings. The J.S. Hamilton team plans to participate in key events dedicated to the cosmetics sector, providing a space for discussions on regulations, testing, and current market challenges:

  • Cosmetotest – 18–19 March 2026, Lyon (Auditorium Mérieux)

  • in-cosmetics Global – 14–16 April 2026, Paris Expo Porte de Versailles

  • Estetica Expo – 5–7 May 2026, Ptak Warsaw Expo

These events offer a valuable opportunity to exchange experiences, discuss ongoing projects, and plan further activities in the field of product testing and safety.

NEW IN THE LABORATORY: IN VITRO SPF METHOD (ISO 23675:2024)

One of the key projects currently being implemented in our laboratory is the introduction of the in vitro SPF determination method in accordance with ISO 23675:2024. This modern approach to assessing sun protection serves as an alternative to in vivo testing and enables faster, more reproducible, and ethical analyses.

The method is based on the use of PMMA plates simulating the skin surface, automated product application, UV irradiation, and spectrophotometric measurements. Implementation of this method at the J.S. Hamilton Laboratory is planned for Q2 2026.

MARKETING SUPPORT BASED ON INSTRUMENTAL ANALYSIS

In response to market needs, we also offer the possibility of creating advanced image collages that combine professional photography with images generated during instrumental analyses (including VISIA and Miravex Antera). Such visual materials allow for an attractive and credible presentation of product performance and can be used in promotional materials, reports, and marketing campaigns.

HRIPT – START OF NEW DERMATOLOGICAL TESTING SESSIONS

In the first quarter of the year, new sessions of HRIPT (Human Repeat Insult Patch Test) studies will also begin, representing an important element of cosmetic product safety assessment. This test allows for the identification of potential irritant and allergic reactions, particularly in the context of long-term product use.

The nearest planned dates are:

  • Start: 02.02 – Report: 18.03

  • Start: 23.02 – Report: 08.04

Early planning of sample shipment enables smooth test execution in line with the schedule and helps avoid delays in subsequent project stages.


The cosmetics industry is entering the new year with increasing regulatory and quality requirements, as well as a growing emphasis on process efficiency and data reliability. In upcoming COSM publications, we will continue to present regulatory changes, guideline interpretations, and practical testing aspects that may have a direct impact on the safety and compliance of cosmetic products.

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Proven proficiency in contaminant testing of recycled plastics

We are pleased to announce that J.S. Hamilton Poland laboratories have successfully completed the DRRR Proficiency Testing programme conducted for Plastics Recyclers Europe (PRE): “Contaminants in recycled plastic material – Phase 2 (RVEP 259599)”.

Successful completion of both proficiency testing rounds resulted in J.S. Hamilton being included on the list of laboratories accepted by Plastics Recyclers Europe (PRE), available to PRE members.

As part of Phase 2, our specialists correctly identified and performed semi-quantitative evaluation of contaminants intentionally introduced into PP granules, meeting all criteria defined for successful participation. Importantly, the first phase of the programme was also completed with a positive result, confirming consistent performance across both rounds.

Successful participation in DRRR proficiency testing demonstrates our laboratories’ proven capability to identify and evaluate potential contaminants in recycled plastic materials – a critical aspect of compliance with regulatory requirements, including Commission Regulation (EU) 2022/1616.

For manufacturers and recyclers, this means reliable analytical results supported by independently verified laboratory competence, contributing to product safety, regulatory compliance, and market acceptance across Europe.

Professional verification of dietary supplement labels

In the dietary supplement industry, labels play a much greater role than just providing information. They are also a tool for communicating with consumers, an element that builds brand credibility, and – crucially – a legal document that must meet specific requirements. Incorrect labeling can lead to serious consequences: from the need to correct labels, through administrative penalties, to product withdrawal from the market.

That is why professional label verification is not an additional feature-today – it is a safety standard and proof of the manufacturer’s responsibility.

Why is correct labeling so important?

Unlike medicines, dietary supplements do not undergo a registration process with an efficacy assessment. This makes reliable information for consumers all the more important, as it must comply with regulations and be supported by expert knowledge.

A correctly prepared label:

  • protects the product from objections by regulatory authorities,
  • prevents misinterpretation by consumers,
  • reduces the risk of legal disputes,
  • strengthens the credibility of the manufacturer and seller,
  • ensures that the declarations are consistent with the facts.

The label thus becomes an integral part of safety – just like purity and microbiology testing or the labeling of active ingredients.

What do the regulations say? Key requirements that a supplement label must meet

The labeling of dietary supplements is regulated in parallel by:

  • Regulation 1169/2011 (FIC) – general rules for consumer information;
  • Directive 2002/46/EC – specific requirements for supplements;
  • Regulation 1924/2006 – nutrition and health claims;
  • Guidelines of the Chief Sanitary Inspectorate and national legislation.

Key mandatory elements include:

  • correct category name (“dietary supplement”),
  • list of ingredients with form and source,
  • active substances given in appropriate units,
  • recommended serving size,
  • method of use and warnings,
  • information on maximum permissible levels,
  • appropriate health claims,
  • prohibited content: suggestions of therapeutic effects, promises of treatment, declarations inconsistent with EFSA.

In reality, many errors are not due to the bad faith of manufacturers, but to a lack of up-to-date knowledge about changing regulations. It is in this area that a professional audit provides the greatest value.

How does label verification work at J.S. Hamilton?

Labeling audits are conducted by a team of food law specialists and food technologists who analyze labels from both a legal and practical perspective.

We check among others:

  1. Compliance with current EU and Polish regulations

Each element of the declaration is compared with the applicable regulations.

  1. Compliance of declared values with laboratory test results

The label cannot declare values that are not confirmed by analyses.

  1. Correct use of nutrition and health claims

We verify acceptable wording in accordance with the EFSA register.

  1. Correctness of active ingredient labeling

Units, chemical forms, conversions, extract standardizations.

  1. Mandatory warnings and instructions for use

In accordance with dietary supplement requirements and good industry practice.

  1. Visual communication elements

We avoid suggesting medicinal properties, risky associations, and inconsistent graphics.

The result is a complete expert opinion that the manufacturer can use as part of their quality documentation, including in the event of an inspection.

The most common errors we detect:

  • health claims that are not allowed to be used,
  • incorrect calculations of active ingredients,
  • lack of mandatory warnings,
  • incorrect naming of chemical forms,
  • use of illegal marketing claims,
  • inadequate contact details and incomplete information about the manufacturer,
  • graphics suggesting therapeutic effects.

Most of these problems can be avoided by performing an audit before printing the label.

Professional label verification — what does the manufacturer gain?

✔ Minimization of legal risk

A correct label means less risk of penalties, inspections, and recalls.

✔ Solid marketing foundation

Health claims are legally compliant but still attractive to the customer.

✔ Consistency between declaration and composition

We verify the label based on the results of supplement composition tests.

✔ Time and cost savings

Correcting a label after printing can be several times more expensive than auditing it before the product is launched on the market.

✔ Protection of brand reputation

Transparency and credibility are becoming a distinguishing feature in a competitive market.

A supplement label is more than just a product’s calling card. It is a document that must be accurate, legally compliant, and reliable. Professional verification helps avoid errors, builds consumer trust, and ensures legal security for the manufacturer.


If you are planning to launch a new dietary supplement or want to assess the compliance of existing labels, J.S. Hamilton’s experts will prepare a comprehensive, professional labeling assessment for you.

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Year-end summary of J.S. Hamilton cosmetology laboratory

The closing year has been a time of intense development, numerous implementations, gaining new knowledge, and strengthening collaborations with industry partners. We are proud to present the key moments and achievements of our team.

Sun Protection – Development of Expertise and Industry Presence

  • Together with PZPK, we created the e-book “Sun Protection (Not Only) in Summer”, which received significant interest from specialists in the field.
  • Once again, we participated in BIPEA inter-laboratory testing (in vivo SPF, in vivo UVA, in vitro UVA), achieving positive results.
  • We participated in the 17th Sun Protection Conference 2025, expanding our knowledge of the latest global trends in UV protection research.

Expanding Research Capabilities

  • From now on, we also report the results of diaper and pet food studies in the form of consumer presentations.
  • We introduced statistical analysis of consumer product testing results, including the use of ANOVA tests for diaper evaluations and other consumer goods.
  • We have implemented a new statistical presentation, including an additional summary table of all tests along with an explanation of the results within the structure of a complete report.

New Services, New Packages, New Equipment

In the past year, we expanded our offerings with several innovations, including:

  • A new testing package: HAIR UV PROTECTION.
  • New services:
    • Breath Freshness Evaluation
    • Comparative statistical analysis of questionnaires
    • Measurement of deep skin hydration
    • TEWL measurement on lips, scalp, and nails
    • Scalp skin elasticity measurement
    • New equipment and service: PRIMOS CR, further developed with innovative 3D analysis – including volume evaluation of lips and under-eye bags (implementation is in progress).
    • We enriched our materials with new collages and visualizations, giving our communication a fresh and modern look.

Audit and Expert Successes of the Year

  • In January, we passed the PCA audit with zero non-conformities, confirming the highest quality level of our work.
  • This year, we successfully passed several audits and client visits, both from Polish and international clients, including a key French supplier, which further strengthens our position in the market as a research partner that meets the highest standards in cosmetic research. In August, we achieved positive results in the Challenge Test DRRR proficiency testing.
  • In the 2024/2025 period, we organized the SILC inter-laboratory tests for the EN13697 method regarding the effectiveness of disinfectants.
  • In December, we participated in the Micro Cosmetica conference, a key event for quality and safety in the industry.
  • As a speaker, we participated in the Polish Cosmetics Industry Association conference during Claims Day, sharing knowledge on the practice of validating claims in cosmetic testing.
  • Over the course of the year, we held about 40 individual expert meetings with clients, a record number that demonstrates how important creating an environment for close collaboration is to us.

This has been a year full of hard work, development, and the introduction of new research opportunities. We thank all our clients, partners, and collaborators for their trust. We look forward to another year filled with challenges and shared successes!

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Dried Fruits and Nuts on the Holiday Table: Heavy Metals and Mycotoxins. What Should Producers Know?

During the holiday season, consumers are particularly keen to reach for dried fruits and nuts: nuts, dried fruits, cake mixes, muesli and “healthy snacks”. These products are associated with naturalness, high quality and family tradition, which is why expectations for their safety are particularly high. At the same time, it is precisely in this product category that the risk of chemical contamination lurks, such as: heavy metals and mycotoxins, which, although invisible to the naked eye, can have real consequences for consumer health and producer reputation. 

Why Do Heavy Metals and Mycotoxins Appear in Dried Fruits and Nuts? 

Heavy metals such as lead, cadmium, inorganic arsenic and mercury are present in the natural environment and can enter food from contaminated soil, water, air or feed. In dried fruits and nuts, they appear primarily as a result of absorption of heavy metal compounds by plants from contaminated environments. The drying process causes an increase in the concentration of these contaminants, which can further lead to exceeding safety standards in the final product. 

Mycotoxins are toxic metabolites of molds that develop on plant raw materials when cultivation, drying or storage conditions are not met. In the case of dried fruits and nuts, aflatoxins (especially B1) produced by Aspergillus fungi, mainly of the species flavus and parasiticus, and ochratoxin A produced by fungi of the genus Aspergillus and Penicillium are particularly important. 

A common feature of heavy metals and many mycotoxins is that health effects can result from long-term exposure to small doses, rather than from single high exposures. From the producer’s perspective, this means the need for continuous control, not one-time verification. 

EU Regulations: What Do the Regulations Require? 

The content of chemical contaminants in food, including in dried fruits and nuts, is regulated primarily by Commission Regulation (EU) 2023/915 and its subsequent amendments. This document specifies the maximum allowable levels for, among others: heavy metals and selected mycotoxins in individual food groups. 

In the area of heavy metals, particularly important for dried fruits and nuts are the limits for cadmium and lead in nuts, oilseeds, dried fruits, cocoa and grain products. The regulations differentiate the values depending on the type of raw material. 

With regard to mycotoxins, the regulation defines, among other things, the allowable levels of aflatoxin B1 and the sum of aflatoxins in nuts and dried fruits intended for direct consumption, as well as separate thresholds for raw materials subject to sorting or other physical processing. The situation is similar in the case of ochratoxin A in dried fruits and nuts – different values apply to raw materials and different to finished products on store shelves. 

When developing quality specifications for raw materials and finished products, it is crucial to refer each time to the current wording of the regulation and its annexes, as the limit values may change with new risk assessments. 

Where Do Mycotoxins Come From in Dried Fruits and Nuts? 

Mycotoxins do not appear “out of nowhere” – they are the result of the development of specific mold species on the raw material. In practice, their development most often occurs when: 

  • crops of nuts or fruits mature or are left in the field under conditions conducive to moisture accumulation, 
  • the drying process is too slow or conducted at inappropriate temperatures, 
  • raw material is stored too long in silos or warehouses with elevated humidity, 
  • water vapor condensation occurs in containers and collective packaging during transport. 

In the case of dried fruits and nuts, an additional challenge is the long supply chain – often including cultivation outside the EU, long transport, repackaging and mixing of raw materials from different sources. This means that the level of mycotoxins is influenced not only by the producer of the final mix, but by every participant in the supply chain – from the farmer, through the dryer and warehouse, to the distributor. 

Heavy Metals in Dried Fruits and Nuts: Environment and Supply Chain 

Heavy metals enter raw materials primarily from soil and water, in which trace but persistent amounts are present. They can also come from industrial emissions, historical contamination of agricultural land or improper waste management in crop cultivation areas. 

In the production of dried fruits and nuts, the risk increases when: 

  • raw materials come from regions with elevated environmental contamination, 
  • there is no systematic verification of new suppliers for heavy metal content. 

This is why supplier assessment, testing of raw materials upon receipt and periodic audits become an element of real risk management, not just a formality of the quality department. 

How Are Heavy Metals and Mycotoxins Tested in Dried Fruits and Nuts? 

The determination of heavy metals requires the use of sensitive techniques that allow detection of very low concentrations in complex matrices such as nuts or dried fruit mixes. In practice, inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma optical emission spectrometry (ICP-OES) are mainly used, allowing simultaneous determination of multiple elements in a single sample. 

At J.S. Hamilton, we analyze mycotoxins mainly using liquid chromatography coupled with mass spectrometry (LC-MS/MS). It is important to take a representative sample and prepare the sample for testing, taking into account the heterogeneity of such products as nut and dried fruit mixes, so that the result truly reflects the level of contamination in the entire batch. 

What Do Test Results Mean for Dried Fruit and Nut Producers? 

For producers, importers and store brands, test results are not just numbers in a test report – they are concrete risk management tools and a way to build competitive advantage. They allow: 

  • confirming the safety and compliance of batches with EU legal requirements, 
  • monitoring the stability and repeatability of processes over time, 
  • quickly identifying the source of the problem (raw material, warehouse, transport) and implementing corrective actions, 
  • communicating to customers and trading partners a real, not declarative approach to food safety. 

In the dried fruits and nuts segment, and particularly intensively rotating during the holiday season – regular testing of heavy metals and mycotoxins is not just about meeting formal requirements. It is an investment in consumer trust, brand protection and a smooth holiday season, when nobody has time for quality crises. 

J.S. Hamilton offers accredited testing of heavy metals and mycotoxins in dried fruits and nuts and other food products, supporting producers in meeting EU legal requirements and securing the holiday season in terms of quality and safety. 

 

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Microbiological safety of dietary supplements – what does a manufacturer need to know?

Dietary supplements are one of the fastest growing segments of the health product market. With their growing popularity, expectations regarding their safety are also growing, both among consumers and regulatory authorities. One of the key areas of control is microbiological safety, which affects not only the quality but also the health of people who use supplements.

At J.S. Hamilton, we regularly support manufacturers in risk assessment and microbiological testing of supplements, helping them to meet legal requirements and maintain a high standard of safety for their products.

Why is microbiology important in supplements?

Dietary supplements – especially those based on plant, fermented, or natural raw materials – can be exposed to microbiological contamination at every stage of the process:

  • during harvesting and storage of raw materials,
  • during transport and packaging,
  • during production,
  • during storage of the finished product.

Contamination can include pathogenic bacteria, fungi, or microorganisms that affect product stability.

Which microorganisms are most commonly tested for?

The most important microbiological parameters in dietary supplements include:

  1. Salmonella spp.

Their presence is must be fully prevented. Salmonella contamination of raw materials is one of the most serious health risks.

  1. Escherichia coli

Indicates fecal contamination and poor hygiene conditions.

  1. Staphylococcus aureus

A bacterium capable of producing toxins that can cause food poisoning.

  1. Molds and yeasts

Particularly important in plant and probiotic supplements — their excess affects the stability and shelf life of the product.

  1. Total aerobic microorganisms (TAMC/TYMC)

A parameter indicating the overall microbiological quality of the preparation.

Legal requirements and quality standards

Although dietary supplements are not high-risk foods, they are subject to detailed regulations regarding microbiological purity. Manufacturers should base their practices on:

  • European Commission guidelines,
  • pharmacopeial specifications (e.g., Ph. Eur. monographs),
  • their own risk analyses,
  • documentation from raw material suppliers.

Regular microbiological testing is not only a legal requirement, but above all an element of responsibility for consumer safety.

How does J.S. Hamilton test the microbiology of supplements?

In our laboratories, we perform a full range of microbiological tests in accordance with current market requirements and regulations. We use methods that are:

  • accredited,
  • validated for the specific nature of supplements,
  • compliant with ISO, the European Pharmacopoeia, and EU guidelines.

This provides manufacturers with reliable and unambiguous results that support supplier verification processes, the introduction of new formulas, and production batch control.

What advantage does microbiological control bring to the manufacturer?

  • greater product safety and stability,
  • protection against complaints and recalls,
  • compliance with inspection requirements,
  • support in the development of quality systems,
  • better control of plant and fermented raw materials.

The microbiological safety of dietary supplements is fundamental to their quality. A properly planned testing program – based on risk analysis and regular inspections—enables manufacturers to supply the market with safe, stable products that comply with legal requirements.

If you need comprehensive support in microbiological testing of dietary supplements, J.S. Hamilton laboratories are at your disposal.


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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Contaminants in Pet Food. The Safety of Food for Our Pets

Why does the topic of contamination in pet food still surprise manufacturers and owners?

At first glance, kibble or canned dog food is just… food. However, what is invisible – trace amounts of mycotoxins, heavy metals, pesticide residues, dioxins, or pathogens – can turn a daily meal into a health threat for your animal. That’s why control and analysis are not a luxury, but a fundamental part of the manufacturing and distribution of pet food.

The Scale of the Problem and Why We Can’t Assume “It’s Just Pet Food”

Contaminants in feeds and pet foods come from various sources: plant and animal raw materials can already contain pesticide residues, mycotoxins, or heavy metals when received at the facility; the production process and storage can introduce additional contaminants (e.g. through contact with contaminated packaging, production lines, or improper additives). Additionally, importing raw materials from regions with different agricultural standards increases the risk. The consequences may include acute poisoning, chronic health problems in animals, and also risk to humans in case of improper handling (e.g. contamination with zoonotic bacteria).

Quality control in pet food production must therefore combine the assessment of raw materials, processes, and the finished product – this is not only the responsibility of manufacturers but also analytical laboratories, inspection authorities, and distribution networks. EU and national laws set out frameworks regulating safety requirements for feeds and pet foods.

Main Categories of Contaminants Found in Pet Food

Below is an overview of the most important groups of contaminants – those that most often appear in quality control and have the greatest health significance.

  1. Mycotoxins (aflatoxins, ochratoxin A, DON, fumonisins)
    Mycotoxins are toxic metabolites of molds (mainly Aspergillus, Fusarium, Penicillium), which may be present in grains, seeds, and plant raw materials used in food. In animals, symptoms depend on the type of mycotoxin, dose, and duration of exposure – from digestive disorders and immune suppression to liver damage and cancer development (e.g. in the case of aflatoxins). The risk is particularly significant in poorly stored raw materials or those harvested under unfavorable weather conditions. Risk assessment institutions (including the European Food Safety Authority – EFSA) continuously monitor the incidence and impact of mycotoxins in the food chain.
  2. Heavy metals (lead, arsenic, cadmium, mercury)
    Heavy metals may derive from contaminated environments, seeds, fish (e.g. mercury), fertilizers, or mineral additives. Long-term exposure even to low doses can lead to accumulation in the body and result in chronic health problems.
  3. Pesticide and insecticide residues
    Chemical residues used in agriculture can enter feeds and food, especially if the raw materials come from intensively cultivated fields. Although many substances have established residue limits, their presence requires monitoring, especially in ingredient blends and with raw materials imported from regions with different agrotechnical practices.
  4. Dioxins, PCBs, and polycyclic aromatic hydrocarbons (PAHs)
    Substances that are difficult to remove, accumulated in fats – may appear in animal raw materials (e.g. fats, fish meal) as a consequence of incorrectly conducted production processes or environmental contamination. They have the potential for long-term toxic effects – including carcinogenic and immunotoxic effects. Studies and risk assessments in the EU also include these groups of contaminants.
  5. Biological contaminants: bacteria, molds, and viruses
    Salmonella, Listeria, E. coli, or some parasites may end up in food, especially in wet products or under poor thermal processing and packaging conditions. The threat concerns both animal health (acute infections) and – when it comes to specific pathogens – human health through handling food. Hence the requirements for hygiene and appropriate testing before releasing a product onto the market.
  6. Adulteration (e.g. melamine)
    Examples from the past show that adding substances to “enhance” nutritional value (specifically “protein content”) can lead to serious health crises. Reliable testing of composition and identification of protein sources are thus extremely important in this context.

Legal Framework: Which Regulations Apply to Pet Food?

Pet food is formally classified as feed. In the European Union, the main legislation producers should be aware of includes, among others, regulations covering feed hygiene, market placement requirements, and limits for certain contaminants. Key elements:

  • Regulations on the marketing and use of feed (including Regulation (EC) No 767/2009) – sets out general rules on placing feed on the market, labeling, and user information.
  • Regulations concerning feed hygiene and production requirements (including Regulation (EC) No 183/2005 and guidelines for its application). These regulations set obligations related to HACCP systems, registration, and inspection of feed producing plants.
  • Acts setting maximum levels of certain contaminants (e.g. Directive 2002/32/EC of the European Parliament and of the Council of 7 May 2002 laying down maximum levels for undesirable substances in animal feed, including aflatoxin B1, dioxins, or metals). Commission rules set limits for specific contaminants, and EFSA provides scientific risk assessment.

In Poland, the classification, supervision, and detailed implementation rules for feed law are supplemented by national institutions (e.g. Veterinary Inspection) – manufacturers and distributors are advised to be familiar with local guidelines and inspection practices.

Research Methods: How Do We Test for Contaminants and Why Does It Work?

Laboratories analyzing pet food use a wide range of techniques. The choice of method depends on the goal of the analysis (quantitative/qualitative), type of matrix (dry food, canned, raw material), and required sensitivity.

  1. LC-MS/MS (high-performance liquid chromatography with tandem mass spectrometry)
    A commonly used method for detecting and quantifying mycotoxins, pesticide residues, and a range of toxic metabolites. LC-MS/MS is highly sensitive, selective, and allows simultaneous determination of multiple analytes. It is the “method of choice” for testing pesticide and toxin residues.
  2. GC-MS and GC-MS/MS (gas chromatography-mass spectrometry or tandem mass spectrometry)
    Suitable for the determination of volatile and semivolatile substances and some organic contaminants (e.g. PAHs). Often used in the analysis of pesticide residues or compounds formed during technological processes.
  3. ICP-MS / ICP-OES (atomic plasma techniques)
    Used to determine heavy metals at very low concentrations (Pb, Cd, As, Hg). ICP-MS provides the sensitivity needed to assess compliance with permissible levels.
  4. Microbiological and molecular methods (culture, PCR, rapid detection methods)
    For detecting Salmonella, Listeria, or other pathogens, both classical cultures and rapid PCR/real-time PCR tests are used, which allow fast identification and confirmation of results. Production hygiene control also requires regular environmental and finished product testing.

The GMP+ system is one of the most recognized and rigorous standards in the European feed sector. It covers both quality requirements and complete safety across the supply chain – from raw materials, through production, to transport and storage. It is not only a set of procedures, but a comprehensive risk management system aimed at one goal: guaranteeing that animal feed is free from chemical, physical, and microbiological hazards.

That’s why it’s so important that the J.S. Hamilton laboratory is officially registered in the GMP+ system for the identification of critical chemical contaminants. This registration confirms that our testing methods, equipment, validation processes, and team competence meet or exceed industry standards. Critical chemical contaminants in the GMP+ system include:

  • Aflatoxin B1
  • Dioxins
  • Dioxin-like PCBs
  • Non-dioxin-like PCBs
  • Heavy metals: cadmium, arsenic, lead, mercury
  • Fluorine
  • Pesticides

In the area of other chemical contaminants, accreditation in accordance with the standard is required.

In practice, this means that our clients can benefit from tests that are accepted in international feed trade and provide a solid foundation for compliance with legal requirements and quality audits. GMP+ is a real guarantee of safety that we build together at every stage of our analyses.

Practical Example: How a Laboratory Verifies Suspected Mycotoxin Contamination

  1. Receipt of samples at the laboratory – delivering a representative sample is key (adequate amount, correct collection method, and transport conditions)
  2. Performing analyses – quantitative determination using appropriate analytical techniques
  3. Test report – in addition to the results, comparison to criteria set out in law is possible.

This scheme enables fast and reliable determination of whether a problem exists, its scope, and action steps to undertake.

Conclusions – What Does This Mean for Manufacturers, Distributors, and Pet Owners?

  1. There is no such thing as “zero risk”- what we have is risk management. Raw material control, regular testing, proper hygiene systems (HACCP/GMP), and cooperation with an accredited laboratory are the foundation. EU and national regulatory frameworks set minimum requirements; best practices must go further.
  2. Raw materials are where the fight for safety truly begins. Supplier control, certificates, monitoring of seasonal materials, and a plan for preliminary tests minimize the risk of contaminants entering the process.
  3. Laboratory testing = certainty of action. Using appropriate analytical methods (LC-MS/MS, GC-MS, GC-MS/MS, ICP-MS, PCR) allows for a reliable assessment and helps avoid false alarms.
  4. Transparency and communication with the customer build trust. Access to test results (e.g. as part of contractor audits) and swift response in case of a problem are elements of responsible market strategy.

Solution: Specific Steps That Can Be Implemented in a Month, Quarter, and Year
Below is a practical action plan for pet food manufacturers who want to reduce contamination risk and demonstrate this to customers.

Within 1 month (quick operational actions):

  • Ensure sampling procedures are up to date and staff are trained – a representative sample is 50% of analytical success.
  • Create a list of critical raw materials and run laboratory tests for the most important ones.
  • Check supplier documentation and request analytical certificates for new batches.

Within 3 months (systematics and monitoring):

  • Develop a periodic testing plan (e.g. quarterly LC-MS/MS tests for selected mycotoxins and ICP-MS for metals).
  • Order an audit of production and storage hygiene (drying conditions, humidity, inventory rotation).
  • Establish procedures for handling non-compliant results (e.g. batch quarantine, supply chain tracing, communication with customers and authorities).

Within 12 months (strategy and communication):

  • Implement a quality system compliant with relevant standards (e.g. GMP+, own safety KPIs).
  • Maintain cooperation with an accredited laboratory (e.g. contract test program, rapid reporting, assistance with result interpretation).
  • Be transparent toward clients: publish selected results and describe control procedures (this builds market advantage).

Most Frequently Asked Questions from Producers – Practical Answers

Do I have to test every package of food?
No – a reliable control plan is based on representative sampling and risk analysis. Each batch should have a specific sampling scheme tailored to production and raw materials.

How often should seasonal raw materials be tested?
The more variable the material quality (e.g. grains from different suppliers), the more often – at least with each new delivery batch and during high-risk seasons (post-drought, heavy rains).

Do laboratory results have legal validity?

Accredited laboratory results are the basis for technical and legal decisions (e.g. batch withdrawal). Depending on the country and situation, authorities may require such documents during inspections.

Pet food safety is a multi-layered issue: it starts in the field and ends in the pet’s bowl. Good production practices, conscious supply chain management, and reliable laboratory testing are the only way to minimize risk and build lasting customer trust.

If you want to move from theory to practice, J.S. Hamilton Poland laboratories offer a wide range of tests using highly sensitive techniques (including mycotoxins, metals, pesticide residues, microbiological studies), as well as result interpretation. Contact us – we will help you construct a testing program tailored to your raw materials and production processes.

 

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

Nutrition Labelling under Regulation (EU) No 1169/2011

Mandatory nutrition declaration on food labels

Providing nutrition information on food labels, in accordance with Regulation (EU) No 1169/2011 of the European Parliament and of the Council, is mandatory for most food products intended for sale to the final consumer. The aim of this regulation is to ensure consistent presentation of nutritional data across the European Union and to enable consumers to make informed dietary choices.

Average nutritional values – how to determine them

It should be noted that the nutritional values declared on the packaging must be average values, determined on the basis of analytical data, literature sources, or recipe calculations, in line with good practice and considering typical variations in production.

Elements of the mandatory nutrition declaration

The mandatory nutrition information generally applies to food in the form in which it is sold and must include a declaration of:

  • energy value
  • fat
  • saturates
  • carbohydrates
  • sugars
  • protein
  • salt

Voluntary information – when can the nutrition table be expanded?

This declaration may voluntarily be supplemented with data on one or more of the following:

  • mono-unsaturates
  • polyunsaturates
  • polyols
  • starch
  • fiber
  • vitamins or minerals present in significant amounts

Rules for presenting vitamins and minerals

If the nutrition declaration includes vitamins or minerals, the percentage of their reference intake values must also be provided, according to Annex XIII, Part A point 1 of Regulation (EU) No 1169/2011. These values must be expressed per 100 g or 100 ml and per portion or consumption unit (if declared).

Expression of nutritional values per 100 g / 100 ml and per portion

The energy value and amounts of nutrients must be expressed per 100 g or 100 ml of the product. Additionally, values may, on a voluntary basis, be provided per portion or consumption unit that is easily recognisable by the consumer, provided that the portion or unit size and the number of portions in the package are clearly indicated on the label.

Format of presenting nutritional information

Nutrition information should be presented in tabular form, with numerical values in columns, in the order specified in Annex XV to Regulation (EU) No 1169/2011. If label space is insufficient, a linear format may be used, but voluntary information cannot be provided at the expense of mandatory information.

Reference Intake (RIV) values – how to use them

On a voluntary basis, nutrition values may also be expressed as a percentage of the Reference Intake (RIV) for adults. RIV percentages may be provided per 100 g/100 ml and/or per portion or consumption unit. A mandatory statement must appear near the RIV values: “Reference intake of an average adult (8 400 kJ/2 000 kcal).”

Front-of-pack nutrition information

Manufacturers may voluntarily repeat part of the mandatory nutrition information on the front of the pack to support consumer understanding. This applies only to energy, saturates, sugars, and salt. It is not permitted to repeat other nutrient information, such as protein content, as part of the front-of-pack nutrition declaration.

Importance of accurate nutrition declarations

Regulation (EU) No 1169/2011 establishes precise requirements for nutrition declarations, ensuring consistency and transparency across the EU market. For manufacturers and entities responsible for labelling, it is both a legal obligation affecting product compliance and an essential element of transparent communication with consumers. Accurate nutrition information enables consumers to make informed food choices.

Most common mistakes in nutrition declarations

Despite the regulation being in force since 2014, incorrectly labelled products can still be found on the market, including errors in data presentation and the use of RI values.

J.S. Hamilton Poland – laboratory services

At J.S. Hamilton Poland, we verify food labelling content, prepare correct nutrition declarations, and support compliance with current legal requirements and regulatory practice. If you have concerns regarding the correct labelling of your products, including nutrition declarations, we invite you to contact us for a nutrition label review.

 

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The administrator of personal data is J.S. Hamilton Poland Sp. z o.o. with headquarters in Gdynia, ul. Chwaszczyńska 180, 81-571 Gdynia. We have appointed a Data Protection Officer who can be contacted by letter or by e-mail: iodo@jsh.com.pl

New Standard PN-EN IEC 62368-1 Added to PCA Accreditation Scope AC 149

We are pleased to announce that the Certification Body of J.S. Hamilton Poland has extended the scope of its PCA accreditation (No. AC 149) to include the PN-EN IEC 62368-1 standard, which defines safety requirements for audio/video (AV), information technology (IT), and telecommunication (ICT) equipment. 

The PN-EN IEC 62368-1 standard merges the previous EN 60950-1 and EN 60065 standards, introducing a unified and modern approach to the safety assessment of electronic equipment. It is based on the concept of Hazard-Based Safety Engineering (HBSE), which focuses on identifying and controlling potential sources of risk to ensure user safety. 

Why is  PN-EN IEC 62368-1 important for manufacturers? 

The new approach provides: 

  • Increased user safety through systematic hazard identification and risk assessment. 
  • A simplified certification process, as one standard replaces two, facilitating the design and market introduction of convergent devices such as smart TVs, routers, and multimedia systems. 
  • Greater design flexibility, since the standard defines safety objectives rather than prescriptive technical solutions. 
  • Compliance with European and global market requirements, as EN IEC 62368-1 is harmonized with the Low Voltage Directive (LVD) and widely recognized internationally. 

What this means for our Clients 

The extension of our accreditation confirms J.S. Hamilton’s competence in testing and certification of electronic products in accordance with the PN-EN IEC 62368-1 standard.

This enables us to provide even broader support to manufacturers in the areas of conformity assessment, safety testing, and product certification, ensuring compliance with legal requirements and facilitating market entry in both the European Union and global markets. 

 

If you have any questions or concerns, J.S. Hamilton Experts are at your disposal.

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High-Protein Products Market — Trend and Availability

The functional food market is developing at a rapid pace, and high-protein products have become one of the hottest nutritional trends in recent years. Today, you can find almost everything in a “protein” version on store shelves — from bars and yogurts to breakfast cereals and protein drinks. Consumers increasingly reach for products labeled “high protein” because they associate them with something healthy, valuable, and “fit.”

The Importance of Protein in the Diet

Consuming protein in the daily diet is extremely important. Alongside carbohydrates and fats, protein is a macronutrient essential for the proper functioning of the body, especially in a high-protein diet. It serves various functions in the body, including supporting muscle growth and regulating metabolic processes. It plays structural roles (tissues, muscles), regulatory roles (enzymes, hormones), and energetic roles (4 kcal/g), making its dietary role enormous.

The body’s protein requirements are not fixed and depend on many factors — primarily age, body weight, physical activity, and health status. General dietary guidelines suggest that adults should consume 0.8–1.0 g of protein per kilogram of body weight per day to maintain adequate protein levels in the diet. Physically active individuals or those in recovery may need much more, even up to 2.2 g/kg of body weight per day.

Factors Influencing Protein Requirements

The broad functionality of protein is likely the reason for its recent surge in popularity within the context of high-protein diets. Products on the market labeled as “protein” or “high-protein” must meet specific criteria regarding protein content. According to the EU Regulation (EC) No. 1924/2006 on nutrition and health claims:

  • “Source of protein” may be used if at least 12% of the energy comes from protein.
  • “High protein” may be used if at least 20% of the energy comes from protein.

Thus, what matters is not only the total protein content but also its proportion in the overall energy value of the product. In practice, a high-protein product should provide approx. 5 g of protein per 100 kcal to support muscle mass development. Of course, the absence of the claim “high protein” on the label does not mean that the product fails to meet this requirement. Nutrition claims are voluntary, and it is up to the manufacturer to decide whether to include them in labeling when conditions are met.

Natural Protein Sources vs. Fortified Products

Among the wide range of “high-protein” products on the market, we find both those naturally rich in protein (such as meat, dairy, and legumes) and those fortified with protein during production. Most often, protein fortification involves the addition of whey protein concentrates and isolates (WPC, WPI) or plant proteins such as soy, pea, rice, and hemp protein.

Supplementation and Protein Additives (WPC, WPI, Plant Proteins)

From a nutritional perspective, a “high-protein” product may have a composition similar to its typical counterpart, only with added protein — but not always. To maintain consumer-acceptable taste and texture, producers often need to modify product formulas.

Formula Modifications and Their Nutritional Consequences

In processed protein-fortified products, we often find added sugars (e.g., glucose-fructose syrup), saturated fats (e.g., palm oil or hydrogenated fats), or food additives (sweeteners, colorants, thickeners). The nutritional value of such modified products may differ significantly from that of foods naturally rich in protein. However, they should not be automatically disqualified just because they are manufactured rather than naturally occurring. In nutrition, balance is key — a varied and well-balanced diet should remain the foundation.

How to Read High-Protein Product Labels

When choosing high-protein products, it is worth paying attention to several label aspects that allow for informed decisions regarding protein intake. It is recommended to check:

  • Ingredient list — should be short and clear;
  • Energy value — does the kcal content match our nutritional needs;
  • Protein content and source — optimally 15–25 g of complete protein per serving, crucial in a high-protein diet;
  • Sugar and saturated fat content — the less, the better.

A Balanced Evaluation of “High-Protein” Products — Practical Guidelines

It is difficult to give a definitive assessment of products labeled “high protein.” These products are undoubtedly a “hit” in recent years, gaining popularity in the food market. When chosen wisely, consumed in moderation, and complementing a well-balanced diet, they can be an attractive nutritional option and should be treated as such. They should not be dismissed as mere marketing tricks to boost sales. They are not pure “hype.” Instead, they can serve as practical tools supporting dietary goals — provided they are used consciously and in moderation.

On the other hand, if treated as a “magic solution” and justification for poor dietary choices simply because they are labeled “protein,” they may indeed be perceived as “hype” being sold to consumers.

Summary: Conscious Choice and Consumer Education

A “high-protein” product makes sense only when accompanied by conscious consumer choice, education, and awareness of the protein products available on the market. This is why reading labels carefully, checking ingredients, and verifying nutritional values are essential to making informed purchasing decisions about protein intake.

Laboratory Testing — Supporting Informed Choices

Conscious consumers increasingly reach for products labeled “protein.” For such claims to be credible, proper verification is essential.

At J.S. Hamilton laboratories, we provide comprehensive food testing, including:

  • Determination of protein content and nutritional value,
  • Verification of compliance with food law requirements,
  • Qualitative and quantitative analyses for producers and distributors.

Thanks to this, producers can confirm their declarations, and consumers can be sure they are choosing safe products consistent with labelling.

 

If you have any questions or concerns, J.S. Hamilton Experts are at your disposal.

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Pet food as a response to the growing needs of our pets

Since prehistoric times, humans have domesticated many species of animals, both companion animals and those of economic importance. Among human companions, dogs and cats are the most popular, but ornamental birds, small mammals, including rodents, ornamental fish, and amphibians, reptiles, and invertebrates, most often kept in terrariums, also constitute a very large group. The annual report of the European Pet Food Industry Federation (FEDIAF) published in 2024 shows that in 2022 there were approximately 129 million cats and 106 million dogs living in Europe, including 7.25 million and 8.109 million in Poland, respectively. FEDIAF is committed to promoting responsible pet ownership, animal welfare, the important social role of pets, and respect for sustainable development.

The new role of dogs and cats in human life

Before dogs and cats became primarily human companions, they were mainly associated with a practical function, such as guarding the home or exterminating rodents. Today, the situation is completely different: pets have become full-fledged members of families, to whom attention, time, and quite large budgets are devoted, primarily in relation to caring for their health and proper nutrition.

Conscious choices made by pet owners

It is no surprise that the pet food market is undergoing a real revolution, as more and more conscious owners are choosing high-quality, balanced products tailored to the individual needs of their pets. The pace of life also influences the tendency to reach for ready-made products instead of preparing food for animals by hand. As a result, the pet food market is growing at an impressive rate, and forecasts indicate that it is one of the fastest-growing sectors of the consumer goods industry.

Today, consumers treat pet food not as a simple mass product, but as an investment in the health and well-being of their pets. This is why the premium and super-premium segments are seeing the greatest growth, where the quality of ingredients, transparency of recipes, and tailoring to specific needs are what count. High-protein foods and those inspired by human-grade diets are gaining popularity. At the same time, there is a growing demand for specialized solutions: veterinary foods, products that support immunity, and those tailored to the age and lifestyle of the animal.

Definition of pet food

Pet food is feed used to feed pets, which, according to the definition given in Regulation (EC) No 767/2009 of the European Parliament and of the Council of 13 July 2009 on the placing on the market and use of feed, amending Regulation (EC) No 1831/2003 and repealing Council Directive 79/373/EEC, Commission Directive 80/511/EEC, Council Directives 82/471/EEC, 83/228/EEC, 93/74/EEC, 93/113/EC and 96/25/EC and Commission Decision 2004/217/EC, as amended, means animals that are not used for food production, fed and kept by humans, but not customarily consumed in the Community. One of the FEDIAF guides clarifies this definition, taking into account cultural customs, and indicates the species that are considered pets. Dog chews made from animal by-products or derived products are also classified as feed.

FEDIAF guidelines provide support for pet food manufacturers

The production and distribution of pet food is regulated by numerous legal acts concerning feed quality and safety and is supervised by veterinary inspections. The European Pet Food Industry Federation has developed a number of guidelines and industry guides in accordance with applicable legislation. They are available in English on the FEDIAF website and in Polish on the website of the Chief Veterinary Inspectorate and the Polish Association of Pet Food Manufacturers POLKARMA, which is a member of FEDIAF. These documents include, among others:

  • Guide to good practice for the manufacture of safe pet foods – supports manufacturers in developing a feed safety management system and meeting legal requirements related to the safety and hygiene of the production process;
  • Code of good labelling practice for pet food – a guide to labeling, explaining the applicable legal provisions and providing practical examples. It specifies, among other things, the conditions for mandatory labeling of analytical constituents, which is related to the type of feed and/or the species of animal for which it is intended, and the acceptable tolerances for differences between the constituents declared on the label and the results of laboratory analyses obtained during official controls.
  • Nutritional guidelines for complete and complementary pet food for cats and dogs – provide an overview of scientific data and indicate nutrient levels such as protein, amino acids, fat, fatty acids, minerals, vitamins, taurine, choline, which are essential for meeting nutritional needs, depending on the species and age of the animal, and for some of them, the highest legally permissible levels or nutritional limits, i.e. the highest levels of nutrients that should not cause side effects. The recommended contents are presented in appropriate units per 100 g of dry matter and per 1000 kcal or MJ of metabolic energy;
  • FEDIAF scientific advisory board carbohydrate expert review – defines the role of carbohydrates in pet food and the benefits of their consumption by animals;
  • Nutritional guidelines for feeding pet rabbits – contain recommendations on the nutritional value of pet food for animals of different ages.

Feed testing performed at the J.S. Hamilton Poland Sp. z o.o. Laboratory

The J.S. Hamilton Poland Sp. z o.o. Laboratory performs tests on the content of analytical constituents declared on pet food labels as mandatory information, i.e.: moisture, protein, fat, ash, crude fiber, hydrochloric acid-insoluble ash and minerals (calcium, sodium, phosphorus) required on the packaging of mineral complementary feed mixtures, as well as feed additives, e.g. vitamins and minerals. Other nutrients in feed, such as amino acids and fatty acids, are also determined. Various analytical techniques are used to analyze the above-mentioned parameters, including gravimetric, titrimetric, spectrometric, and chromatographic techniques. The laboratory also verifies the compliance of the test results with the requirements of applicable laws and FEDIAF documents.

 

If you have any questions or concerns, J.S. Hamilton Experts are at your disposal.

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Advanced wrinkle analysis using PRIMOS CR – project implementation successfully completed!

We are pleased to announce the introduction of a new diagnostic service utilizing the PRIMOS CR system. PRIMOS is a state-of-the-art clinical research tool designed for the evaluation of skin microstructure and advanced wrinkle assessment. It provides precise quantitative results for wrinkle depth, length, volume, number, and surface area within the measured zone.

How does PRIMOS CR work?

PRIMOS CR operates using fringe projection technology, also known as phase-shifting profilometry. In this method, a precisely modulated fringe pattern is projected onto the skin surface. As the light pattern becomes distorted by the skin’s microtopography, the system captures these deformations and reconstructs a highly accurate 3D topography of the skin.

Thanks to the implementation of phase-shifting interferometry, PRIMOS CR achieves exceptionally high axial resolution (up to 0.1 μm) and lateral resolution, making it ideal for analyzing fine skin structures and subtle surface changes.

The development of dedicated analytical scripts and the integration of automated data processing through the VECTRA analysis software.

What parameters does PRMOS CR test?

  • Standardized wrinkle assessment (depth, length, volume),
  • Skin roughness analysis based on parameters: Ra, Rz, Rt,
  • Time-lapse comparison of changes (monitoring treatment effectiveness).

These automated scripts also allow for in-vivo comparative studies (before and after treatment), as well as the evaluation of cosmetic product efficacy. This makes PRIMOS CR an invaluable tool in both clinical practice and R&D laboratories.

Book a consultation with our expert Oliwia Kalinowska and tailor a study protocol according to the latest industry standards. Please contact us at cosm@jsh.com.pl.

What do the images generated by PRMOS CR look like?

  • Eye wrinkles:
Subject’s no. X.
Before (D0)
After X days (DX)

 

Subject’s no. Before (D0) After X days (DX)

X.

  • Forehead wrinkles:
Subject’s no. X.
Before (D0)
After X days (DX)

 

Subject’s no. Before (D0) After X days (DX)

X.

 

Our qualified team will provide a suitably selected panel of subjects in accordance with the Client’s requirements.

Ask our experts about research offers using PRIMOS CR.

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