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en-1811-determination-of-nickel-release-from-skin-contact-products
Dermatological & Sensitivity Testing AFNOR BP X30-221 In Vivo Human Skin Testing ProceduresASTM D2979 Assessment of Skin Sensitization PotentialASTM D4236 Labeling of Cosmetic Products for Skin SafetyASTM D6125 Evaluation of Skin Sensitization Using In Vitro ModelsASTM D6977 Evaluation of Skin Contact AllergensASTM E1490 Evaluation of Allergic Contact DermatitisASTM E2711 Human Repeat Insult Patch Test (HRIPT) with Extended ProtocolASTM E2753 Human Repeat Insult Patch Test (HRIPT)ASTM F2312 Evaluation of Patch Test Allergen ReleaseCOLIPA Guidelines for Skin Compatibility TestingEN 16820 Test Method for Skin Sensitization PotentialEN ISO 10993-10 Assessment of Skin IrritationEN ISO 10993-18 Chemical Characterization for Dermal SafetyEN ISO 10993-21 Evaluation of Skin Irritation from Medical Device ExtractsEN ISO 10993-5 Cytotoxicity Testing on Skin CellsEP 5.1.6 Evaluation of Dermatological Safety of CosmeticsFDA 21 CFR 820 Quality System Regulation for Dermal DevicesFDA 21 CFR Part 807 Sensitivity Testing of Topical ProductsFDA Guidance for Dermatological Testing of Topical ProductsFDA Guidance on Dermal Sensitization Risk AssessmentISO 105-A02 Colorfastness to Artificial Light on SkinISO 10993-1 Biological Evaluation of Medical Devices - Dermal AspectsISO 10993-10 Evaluation of Skin Irritation and SensitizationISO 10993-11 Toxicity Testing Related to Skin ContactISO 10993-12 Sample Preparation for Dermal TestingISO 10993-16 Toxicokinetic Testing of Substances in Dermal ExposureISO 10993-17 Toxicological Risk Assessment for Dermal ProductsISO 10993-19 Evaluation of Allergic Contact Dermatitis in Skin ProductsISO 10993-20 Dermal Toxicology Testing MethodsISO 10993-22 Evaluation of Sensitization from Skin Contact DevicesISO 10993-23 Evaluation of Phototoxicity and PhotoallergyISO 11137 Sterilization Validation of Dermal DevicesISO 11930 Preservative Effectiveness for Sensitive Skin ProductsISO 14155 Clinical Investigation of Medical Devices on SkinISO 15223-1 Symbols for Dermal Medical DevicesISO 15223-1 Symbols for Indicating Skin Contact in Medical DevicesISO 16128 Guidelines on Natural and Organic Cosmetic IngredientsISO 16128-1 Guidelines on Natural and Organic Cosmetics Part 1ISO 16128-2 Calculation of Natural Ingredient Content in Skin ProductsISO 16128-3 Methodologies for Determining Organic Content in Skin CareISO 16134 Human Repeat Insult Patch Test GuidanceISO 16134-2 Guidance for Patch Test Interpretation in Skin TestingISO 17516 Microbiological Limits for Skin ProductsISO 21404 Testing for Skin Contact AllergensISO 21486 Risk Assessment for Skin Contact MaterialsISO 22444 Measurement of Skin Moisture ContentISO 22715 Labeling Requirements for Skin and Cosmetic ProductsISO 22716 Good Manufacturing Practices for Dermatological ProductsISO 22716-1 Good Manufacturing Practices for Skin Care ProductsISO 23975 Patch Test Protocols for Dermatological ProductsISO 24441 In Vitro Determination of Sun Protection Factor (SPF)ISO 24442 Evaluation of Human Skin Irritation PotentialISO 24443 In Vitro Assessment of Sunscreen Efficacy on SkinISO 24443 In Vitro SPF Testing for SunscreensISO 24443 In Vitro UV Protection Factor Testing for SunscreensISO 24443 UV Protection Testing for Sensitive Skin FormulationsISO 3160-2 Compression Testing on Skin Contact MaterialsISO 3175-4 Analysis of Volatile Components Affecting Skin SensitivityISO 8124-6 Safety Requirements for Toys Affecting SkinISO/TR 16181 Guidelines on Skin Compatibility of CosmeticsISO/TR 16271 Guidelines on Safety Assessment for Skin Contact MaterialsISO/TR 19218 Dermatological Safety Data ManagementISO/TR 19930 Development of Dermal Sensitization AssaysISO/TR 22219 Testing of Skin Barrier FunctionISO/TR 29622 Allergens in Cosmetics and Personal Care ProductsJIS K 5600-5-7 Patch Test Methods for Skin SensitivityOECD TG 405 Acute Dermal Irritation/Corrosion TestOECD TG 406 Skin Sensitization in AnimalsOECD TG 406 Skin Sensitization Testing in AnimalsOECD TG 437 Bovine Corneal Opacity and Permeability Test for Skin SafetyOECD TG 439 In Vitro Skin Irritation Testing for CosmeticsOECD TG 442B Local Lymph Node Assay for Skin SensitizationOECD TG 442C In Chemico Skin Sensitization Assay (DPRA)OECD TG 442D In Vitro Skin Sensitization Assay (KeratinoSens™)OECD TG 442E Human Cell Line Activation Test (h-CLAT) for Skin SensitizationOECD TG 442E In Vitro Skin Sensitization Assay (h-CLAT)USP <151> Evaluation of Skin Irritation for Topical Dosage FormsUSP <151> Skin Sensitization Studies in Pharmaceuticals

Comprehensive Guide to EN 1811 Determination of Nickel Release from Skin-Contact Products Laboratory Testing Service

Provided by Eurolab: Expertise in Laboratory Testing Services

Table of Contents

Standard-Related Information

The EN 1811 Determination of Nickel Release from Skin-Contact Products testing service is governed by the European Standard EN 1811, which specifies the method for determining the nickel release from skin-contact products. This standard is part of the European harmonization process and ensures that manufacturers comply with the safety requirements for consumer products.

The relevant standards that apply to this specific laboratory test include:

  • EN 1811:2014A1:2018 - Determination of Nickel Release from Skin-Contact Products

  • ISO 17252-2:2003 - Consumer Safety Part 2: Safety Requirements for Childrens Cots and Folding Cribs

  • TSE (Turkish Standards Institution) IEC 62341-3-6:2020 - Flexible Printed Circuits Part 3-6: Design, Installation, Testing Made by the Manufacturer, Operation and Maintenance

    • Standard development organizations, such as the International Electrotechnical Commission (IEC), play a crucial role in creating and updating standards to ensure consumer safety.

    Standard Requirements and Needs

    The EN 1811 Determination of Nickel Release from Skin-Contact Products testing is necessary due to the potential health risks associated with nickel exposure. This test is required by various industries, including:

  • Cosmetics

  • Jewelry

  • Fashion accessories

  • Consumer electronics

    • Failure to perform this test can result in product recalls, financial losses, and damage to a companys reputation.

    Test Conditions and Methodology

    The EN 1811 Determination of Nickel Release from Skin-Contact Products testing involves the following steps:

    1. Sample preparation: The sample is prepared according to the standard.

    2. Testing equipment and instruments: Specific equipment, such as a rotating drum, is used for the test.

    3. Testing environment requirements: The temperature and humidity conditions are controlled during the test.

    4. Measurement and analysis methods: The nickel release is measured using techniques such as atomic absorption spectroscopy (AAS).

    5. Calibration and validation procedures: Regular calibration and validation of equipment ensure accurate results.

    Test Reporting and Documentation

    The test report includes:

  • Summary of the test procedure

  • Results and conclusions

  • Recommendations for improvement

  • Certificate of compliance

    • Eurolabs reporting system is electronic, ensuring fast and secure delivery of test reports to clients.

    Why This Test Should Be Performed

    Performing EN 1811 Determination of Nickel Release from Skin-Contact Products testing:

  • Ensures product safety and reliability

  • Complies with regulatory requirements

  • Reduces the risk of product recalls and financial losses

  • Improves customer confidence and trust

  • Enhances international market access and trade facilitation

    • Why Eurolab Should Provide This Service

    Eurolabs expertise in laboratory testing services includes:

  • State-of-the-art equipment and facilities

  • Qualified and certified personnel

  • Accreditation and certification details

  • International recognition and partnerships

  • Quality management systems and procedures

    • By choosing Eurolab for EN 1811 Determination of Nickel Release from Skin-Contact Products testing, clients can expect:

  • Fast turnaround times

  • Competitive pricing and value proposition

  • Technical support and consultation services

    • Industry-Specific Examples and Case Studies

    Eurolab has successfully conducted numerous EN 1811 tests for various industries. For example:

  • A leading jewelry manufacturer required EN 1811 testing for their nickel-plated products.

  • A cosmetics company needed EN 1811 testing for their nail polish products.

    • Conclusion

    The EN 1811 Determination of Nickel Release from Skin-Contact Products laboratory testing service is crucial for ensuring product safety and compliance with regulatory requirements. Eurolabs expertise, state-of-the-art equipment, and quality management systems make us the ideal partner for this testing service. Contact us today to learn more about our capabilities and advantages.

    Additional Resources

    For more information on EN 1811 Determination of Nickel Release from Skin-Contact Products testing or other laboratory services, please visit our website at www.eurolab.com(http://www.eurolab.com).

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