EUROLAB
iso-21702-antiviral-efficacy-testing-of-preservatives
Preservative Efficacy Testing AOAC 2003.07 Challenge Testing for Preservative EffectivenessAOAC 2007.01 Microbial Challenge Testing for PreservativesAOAC 991.14 Microbial Contamination Analysis in Preserved ProductsAOAC 997.02 Challenge Test Method for Preservative EffectivenessASTM D4014 Preservative Testing for Creams and LotionsASTM D5412 Microbial Limits Testing in Preserved CosmeticsASTM D6422 Preservative Effectiveness in Personal Care ProductsASTM E2180 Antimicrobial Activity of Preservative SystemsASTM E2181 Preservative Efficacy Testing for CosmeticsASTM E2315 Preservation Challenge Test for Cosmetic ProductsASTM E2315 Time-Kill Method for Preservative AssessmentASTM E2315-16 Time-Kill Kinetics for Preservative EffectivenessASTM E2316 Microbial Assessment of Cosmetic PreservativesASTM E2317 Antimicrobial Efficacy of Cosmetic PreservativesASTM E2709 Challenge Tests for Preservative SystemsASTM E2799 Antimicrobial Effectiveness Testing for CosmeticsCOLIPA Guidelines for Preservative Efficacy in CosmeticsEN ISO 11930 Microbial Preservation Testing for Personal CareEN ISO 11930 Microbial Quality and Preservation AssessmentEP 2.6.12 Enumeration of Microorganisms in Preserved ProductsEP 2.6.13 Detection of Specified Microorganisms in Preserved ProductsEP 5.1.3 Challenge Test for Preservative EfficacyEP 5.1.4 Microbial Limits in Preserved IngredientsEP 5.1.5 Microbial Quality Control in Preserved FormulationsFDA 21 CFR 701.3 Microbial Contamination Limits in Preserved ProductsFDA 21 CFR Part 700 Microbial Limits for Preserved CosmeticsFDA BAM Chapter 23 Microbial Pathogen Detection in Preserved ProductsFDA Cosmetic Microbiological Testing GuidanceFDA Guidance on Preservative Testing for Topical ProductsISO 10993-10 Preservation Efficacy in Dermal ProductsISO 10993-12 Sample Preparation for Preservative TestingISO 11930 Challenge Test of Preservatives in CosmeticsISO 11930 Evaluation of Preservative Efficacy in CosmeticsISO 11930-1 Preservative Challenge Testing for Rinse-off ProductsISO 11930-2 Preservative Testing of Leave-on CosmeticsISO 11932 Validation of Microbial Methods in Preservation TestingISO 11989 Validation of Microbiological Methods in Preserved ProductsISO 16128 Natural and Organic Cosmetic Ingredient PreservationISO 16128-2 Calculation of Natural Preservative ContentISO 16134-3 Testing of Preservative EffectivenessISO 16212 Detection of Yeasts and Molds in Preserved CosmeticsISO 16212 Mold and Yeast Quantification in Preserved CosmeticsISO 17516 Microbial Limits and Preservation TestingISO 18415 Microbial Challenge Test for Personal Care ProductsISO 18593 Microbial Sampling in Preserved ProductsISO 18593 Microbiological Sampling Methods for Preserved ProductsISO 21148 Detection of Anaerobic Microorganisms in Preserved ProductsISO 21148 Detection of Preservative-Resistant MicroorganismsISO 21149 Enumeration of Aerobic Bacteria for Preservative StudiesISO 21149 Enumeration of Microorganisms in Preserved FormulationsISO 21149-1 Enumeration of Aerobic Bacteria in Preserved FormulationsISO 21150 Detection of Pathogens in Preserved CosmeticsISO 21150-1 Microbial Contamination in Cosmetic Raw MaterialsISO 21404 Testing for Microbial Contamination in Preserved CosmeticsISO 22176 Good Hygiene Practices for Preserved CosmeticsISO 22716 Good Manufacturing Practices for Cosmetic PreservationISO 24434 Enumeration of Aerobic Mesophilic Spores in Preserved ProductsISO 24441 SPF Testing for Preserved SunscreensISO 24442 Enumeration of Aerobic Microbial Spores in ProductsISO 24442 Microbial Spores Enumeration in Preserved ProductsISO 24444 Comparison of Microbiological Test ProtocolsISO 24475 Microbiological Assessment of Preserved Raw MaterialsISO 29621 Categorization of Cosmetic Products by Microbiological RiskISO/TR 19837 Guidelines for Microbiological Risk Assessment of PreservativesISO/TR 19838 Risk Management of Preservatives in CosmeticsISO/TR 19930 Microbiological Test Method Development for PreservativesISO/TR 24476 Selection of Microbiological Test Methods for PreservationISO/TR 29621 Guidelines on Risk Assessment for PreservativesUSP <1227> Validation of Microbial Recovery in Preservative StudiesUSP <1227> Validation of Microbial Recovery in Preservative TestingUSP <1229> Microbial Recovery in Preservative Efficacy TestsUSP <1231> Water Quality for Microbiological Control in Preservative TestingUSP <1625> Microbial Testing of Preserved Topical ProductsUSP <51> Antimicrobial Effectiveness Testing for PreservativesUSP <60> Microbial Limits in Preserved CosmeticsUSP <61> Microbial Enumeration Tests in Preserved Cosmetics

ISO 21702 Antiviral Efficacy Testing of Preservatives: Eurolabs Laboratory Testing Service

ISO 21702 is an international standard that specifies the method for determining the efficacy of antiviral preservatives in coatings, paints, and other materials. This standard is developed by the International Organization for Standardization (ISO) and published as a collaborative effort between various national standards bodies.

Legal and Regulatory Framework

The legal and regulatory framework surrounding ISO 21702 Antiviral Efficacy Testing of Preservatives testing is complex and varied depending on the country, industry, and specific regulations. In general, this testing service is required by regulatory authorities to ensure the safety and effectiveness of products containing antiviral preservatives.

International and National Standards

The following international and national standards apply to ISO 21702 Antiviral Efficacy Testing of Preservatives testing:

  • ISO 21702:2015 - Paints and varnishes - Determination of the efficacy of antiviral preservatives
  • ASTM E2197-14 - Standard Practice for Evaluating Adhesion by Tape Test
  • EN ISO 1519:2004 - Paints and varnishes - Evaluation of the effectiveness of anti-fouling paints against marine fouling organisms
  • TSE (Turkish Standards Institution) - Yönetmelik No. 2015/7 - Paints and varnishes - Determination of the efficacy of antiviral preservatives
  • Standard Development Organizations

    Standard development organizations play a crucial role in developing, revising, and maintaining standards such as ISO 21702. Some notable standard development organizations include:

  • International Organization for Standardization (ISO)
  • American Society for Testing and Materials (ASTM)
  • European Committee for Standardization (CEN)
  • Turkish Standards Institution (TSE)
  • How Standards Evolve

    Standards evolve through a collaborative effort between stakeholders, including industry experts, regulatory authorities, and standard development organizations. This process involves:

    1. Identification of needs and gaps

    2. Development of proposals

    3. Review and approval by standards committees

    4. Publication as an international or national standard

    Standard Numbers and Scope

    The following are the relevant standard numbers and their scope:

  • ISO 21702:2015 - Paints and varnishes - Determination of the efficacy of antiviral preservatives (Scope: This International Standard specifies the method for determining the efficacy of antiviral preservatives in coatings, paints, and other materials.)
  • ASTM E2197-14 - Standard Practice for Evaluating Adhesion by Tape Test (Scope: This standard covers a procedure for evaluating adhesion by tape test)
  • EN ISO 1519:2004 - Paints and varnishes - Evaluation of the effectiveness of anti-fouling paints against marine fouling organisms (Scope: This European Standard specifies a method for evaluating the effectiveness of anti-fouling paints against marine fouling organisms)
  • Standard Compliance Requirements

    Compliance with standards such as ISO 21702 is mandatory in various industries, including:

  • Coatings and paints
  • Pharmaceuticals
  • Cosmetics
  • Medical devices
  • Industry-specific compliance requirements are detailed below:

  • Coatings and paints: Complying with ISO 21702 ensures the efficacy of antiviral preservatives in coatings, paints, and other materials.
  • Pharmaceuticals: Complying with ISO 21702 ensures the safety and effectiveness of pharmaceutical products containing antiviral preservatives.
  • Cosmetics: Complying with ISO 21702 ensures the safety and effectiveness of cosmetic products containing antiviral preservatives.
  • Medical devices: Complying with ISO 21702 ensures the safety and effectiveness of medical devices containing antiviral preservatives.
  • Why This Test is Needed and Required

    ISO 21702 Antiviral Efficacy Testing of Preservatives testing is necessary to ensure the safety and effectiveness of products containing antiviral preservatives. The consequences of not performing this test include:

  • Ineffective protection against viral infections
  • Reduced product performance and shelf life
  • Compliance issues with regulatory authorities
  • Business and Technical Reasons for Conducting ISO 21702 Testing

    Conducting ISO 21702 testing provides several business and technical benefits, including:

  • Ensuring the safety and effectiveness of products containing antiviral preservatives
  • Complying with regulatory requirements
  • Enhancing product performance and shelf life
  • Building customer confidence and trust
  • Industries and Sectors that Require This Testing

    The following industries and sectors require ISO 21702 Antiviral Efficacy Testing of Preservatives testing:

  • Coatings and paints
  • Pharmaceuticals
  • Cosmetics
  • Medical devices
  • Biotechnology
  • Risk Factors and Safety Implications

    Conducting ISO 21702 testing helps to mitigate the risk factors associated with viral infections, including:

  • Reduced product performance and shelf life
  • Compliance issues with regulatory authorities
  • Loss of customer confidence and trust
  • Standard Requirements and Needs

    The following are the standard requirements and needs for ISO 21702 Antiviral Efficacy Testing of Preservatives testing:

  • Complying with regulatory requirements
  • Ensuring the safety and effectiveness of products containing antiviral preservatives
  • Enhancing product performance and shelf life
  • Building customer confidence and trust
  • How to Conduct ISO 21702 Testing

    Conducting ISO 21702 testing involves several steps, including:

    1. Sample preparation

    2. Antiviral preservative application

    3. Exposure to viral challenge

    4. Evaluation of antiviral efficacy

    The following are the equipment and materials required for conducting ISO 21702 testing:

  • Paints and varnishes
  • Coatings
  • Pharmaceuticals
  • Cosmetics
  • Medical devices
  • Biotechnology products
  • Quality Control and Assurance

    Conducting ISO 21702 testing requires a quality control and assurance system to ensure the accuracy and reliability of test results. This includes:

    1. Calibration of equipment

    2. Validation of methods

    3. Training of personnel

    4. Document control

    5. Record keeping

    Standard Operating Procedures (SOPs)

    Developing and implementing SOPs for ISO 21702 testing ensures consistency and reproducibility in test results. SOPs should cover:

    1. Sample preparation

    2. Antiviral preservative application

    3. Exposure to viral challenge

    4. Evaluation of antiviral efficacy

    Record Keeping

    Maintaining accurate records is essential for conducting ISO 21702 testing, including:

    1. Test samples and results

    2. Equipment calibration and maintenance records

    3. Method validation and verification records

    4. Training and qualification of personnel records

    Certification and Accreditation

    Conducting ISO 21702 testing requires certification and accreditation from a recognized third-party organization. This ensures that the laboratory meets the requirements for testing and evaluation.

    Standard Operating Procedures (SOPs) for Certification and Accreditation

    Developing and implementing SOPs for certification and accreditation ensures consistency and reproducibility in test results. SOPs should cover:

    1. Laboratory setup and maintenance

    2. Equipment calibration and maintenance

    3. Method validation and verification

    4. Training and qualification of personnel

    Conclusion

    Conducting ISO 21702 Antiviral Efficacy Testing of Preservatives testing is essential for ensuring the safety and effectiveness of products containing antiviral preservatives. This standard provides a framework for evaluating the efficacy of antiviral preservatives in coatings, paints, and other materials.

    Why This Test is Needed and Required

    ISO 21702 Antiviral Efficacy Testing of Preservatives testing is necessary to ensure the safety and effectiveness of products containing antiviral preservatives. The consequences of not performing this test include:

  • Ineffective protection against viral infections
  • Reduced product performance and shelf life
  • Compliance issues with regulatory authorities
  • Business and Technical Reasons for Conducting ISO 21702 Testing

    Conducting ISO 21702 testing provides several business and technical benefits, including:

  • Ensuring the safety and effectiveness of products containing antiviral preservatives
  • Complying with regulatory requirements
  • Enhancing product performance and shelf life
  • Building customer confidence and trust
  • Industries and Sectors that Require This Testing

    The following industries and sectors require ISO 21702 Antiviral Efficacy Testing of Preservatives testing:

  • Coatings and paints
  • Pharmaceuticals
  • Cosmetics
  • Medical devices
  • Biotechnology
  • Risk Factors and Safety Implications

    Conducting ISO 21702 testing helps to mitigate the risk factors associated with viral infections, including:

  • Reduced product performance and shelf life
  • Compliance issues with regulatory authorities
  • Loss of customer confidence and trust
  • Standard Requirements and Needs

    The following are the standard requirements and needs for ISO 21702 Antiviral Efficacy Testing of Preservatives testing:

  • Complying with regulatory requirements
  • Ensuring the safety and effectiveness of products containing antiviral preservatives
  • Enhancing product performance and shelf life
  • Building customer confidence and trust
  • How to Conduct ISO 21702 Testing

    Conducting ISO 21702 testing involves several steps, including:

    1. Sample preparation

    2. Antiviral preservative application

    3. Exposure to viral challenge

    4. Evaluation of antiviral efficacy

    The following are the equipment and materials required for conducting ISO 21702 testing:

  • Paints and varnishes
  • Coatings
  • Pharmaceuticals
  • Cosmetics
  • Medical devices
  • Biotechnology products
  • Quality Control and Assurance

    Conducting ISO 21702 testing requires a quality control and assurance system to ensure the accuracy and reliability of test results. This includes:

    1. Calibration of equipment

    2. Validation of methods

    3. Training of personnel

    4. Document control

    5. Record keeping

    Standard Operating Procedures (SOPs)

    Developing and implementing SOPs for ISO 21702 testing ensures consistency and reproducibility in test results. SOPs should cover:

    1. Sample preparation

    2. Antiviral preservative application

    3. Exposure to viral challenge

    4. Evaluation of antiviral efficacy

    Record Keeping

    Maintaining accurate records is essential for conducting ISO 21702 testing, including:

    1. Test samples and results

    2. Equipment calibration and maintenance records

    3. Method validation and verification records

    4. Training and qualification of personnel records

    Certification and Accreditation

    Conducting ISO 21702 testing requires certification and accreditation from a recognized third-party organization. This ensures that the laboratory meets the requirements for testing and evaluation.

    Standard Operating Procedures (SOPs) for Certification and Accreditation

    Developing and implementing SOPs for certification and accreditation ensures consistency and reproducibility in test results. SOPs should cover:

    1. Laboratory setup and maintenance

    2. Equipment calibration and maintenance

    3. Method validation and verification

    4. Training and qualification of personnel

    Conclusion

    Conducting ISO 21702 Antiviral Efficacy Testing of Preservatives testing is essential for ensuring the safety and effectiveness of products containing antiviral preservatives. This standard provides a framework for evaluating the efficacy of antiviral preservatives in coatings, paints, and other materials.

    The final answer is: boxed0

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