EUROLAB
ts-en-12353-hygiene-control-of-cosmetic-containers-and-closures
Microbiological Quality Testing AFNOR NF T73-101 Microbial Preservation Testing for CosmeticsANSM Challenge Testing of Natural Cosmetic FormulasANSM Microbiological Control of Non-Sterile Cosmetic ProductsANVISA RDC 481/2021 Microbial Control for Brazilian Cosmetic ProductsAOAC 2003.07 Challenge Test for Cosmetic CreamsAOAC 991.14 Microbial Contamination Detection in Personal Care ProductsAOAC 997.02 Microbial Quality of ToiletriesASTM D4014 Test for Microbial Growth on Lotions and CreamsASTM D5338 Biodegradation and Microbial Interaction in CosmeticsASTM D7983 Testing for Bacterial Endotoxins in Eye-area CosmeticsASTM E1326 Viable Organism Testing in Aerosolized Cosmetic ProductsASTM E2180 Antimicrobial Efficacy Testing of Preservative SystemsASTM E2275 Skin Antiseptic Residual Activity TestingASTM E2315 Time-Kill Assessment of Antimicrobial ActivityASTM E2613 Microbial Analysis of Water Used in CosmeticsASTM E2786 Biofilm Formation in Cosmetic Production EnvironmentsASTM E640 Bacterial Filtration in Cosmetic SpraysASTM F2101 Bacterial Filtration Efficiency of Cosmetic Face MasksCEN/TR 16953 Guidance on Application of ISO Microbial StandardsChina GB 7919 Microbial Limits in Non-Sterile CosmeticsChina GB/T 13531.1 Detection of E. coli in CosmeticsChina GB/T 13531.2 Detection of Pathogenic Bacteria in CosmeticsChina GB/T 13531.3 Microbial Limit in Baby ProductsCOLIPA Guideline for Preservation Efficacy TestingCOLIPA Microbiological Quality Assurance of Cosmetic ProductsEP 2.6.1 Sterility Test for Cosmetic Raw MaterialsEP 2.6.12 Total Aerobic Microbial Count TestingEP 2.6.13 Detection of Designated Microorganisms in CosmeticsEP 2.6.31 Validation of Microbiological Test Methods for CosmeticsEP 5.1.3 Evaluation of Preservative EffectivenessEP 5.1.4 Microbial Limits in Raw Cosmetic IngredientsEPA MB-17 Microbial Contamination Control in Natural FormulasFDA 21 CFR 211.113 Contamination Prevention Procedures for CosmeticsFDA 21 CFR 700.3 Microbial Contamination Limits in CosmeticsFDA BAM Chapter 14 Yeast and Mold Enumeration in Personal Care ProductsFDA BAM Chapter 23 Detection of Bacterial Pathogens in CosmeticsFDA CFSAN Guidelines for Cosmetic Microbiological SamplingFDA CPG Sec. 7120.01 Microbiological Criteria for Finished CosmeticsHealth Canada Compendial Test for Pathogenic Organisms in CosmeticsHealth Canada Cosmetic Microbiological Contamination GuidelinesIndia IS 14642 Microbial Contamination in Toiletries and SkincareIndia IS 4707-2 Cosmetic Ingredients Microbial AssessmentISO 11930 Microbiological Preservation Efficacy TestingISO 11932 Method Validation for Microbial Testing in CosmeticsISO 11989 Microbial Assessment of Eye CosmeticsISO 14502-2 Microbiological Testing of Polyphenol-Rich CosmeticsISO 16212 Quantification of Yeasts and Molds in Cosmetic ProductsISO 17516 Quantitative Limits of Microorganisms in Finished ProductsISO 18415 Detection of Specified and Non-Specified MicroorganismsISO 19007 Preservation Test of Microbial Resistance in Cosmetic WipesISO 21148 Detection of Anaerobic Bacteria in Cosmetic FormulationsISO 21149 Detection of Aerobic Mesophilic Bacteria in CosmeticsISO 21150 Detection of Escherichia coli in CosmeticsISO 22176 Hygiene Requirements in Cosmetic Packaging LinesISO 22716 Microbial Risk Management in GMP Cosmetic ManufacturingISO 22717 Identification of Pseudomonas aeruginosa in Cosmetic ProductsISO 22718 Identification of Staphylococcus aureus in CosmeticsISO 22719 Detection of Candida albicans in Cosmetic ProductsISO 24434 Enumeration of Aerobic Mesophilic Spores in Personal CareISO 24442 Selection Criteria for Challenge Test OrganismsISO 29621 Microbiological Risk Assessment for Low-Risk ProductsISO/TR 19838 Guidance on Risk Management for Cosmetic MicrobiologyISO/TR 24444 Comparison of Microbiological Test ProtocolsISO/TR 24475 Microbiological Assessment of Cosmetic Raw MaterialsISO/TR 24476 Test Method Selection for Cosmetic Product MicrobiologyISO/TS 29621 Categorization of Cosmetic Products Based on Microbiological RiskJIS K 5101 Preservative Efficiency in Japanese CosmeticsJIS L 1902 Evaluation of Antibacterial Activity of Cosmetic TextilesJIS Z 2801 Antimicrobial Efficacy Testing for Surfaces in Cosmetic FacilitiesKFDA Microbiological Safety Evaluation of Korean Cosmetic ProductsKFDA Testing for Microbial Contamination in Imported CosmeticsPh. Eur. 2.6.12 Total Count Test for EmulsionsPh. Eur. 2.6.13 Detection of Pathogens in Powdered CosmeticsSCCS/1564/15 Risk Assessment of Microbiological Contamination in CosmeticsSCCS/1611/19 Safety Levels of Microbial Contaminants in CosmeticsTS 13218 Total Bacteria Count in Cosmetic CreamsTS 13531 Bacterial Safety Testing of Shampoo ProductsTS EN ISO 11930 Preservative Efficacy Test for Personal Care ProductsTS EN ISO 16212 Mold and Yeast Count in Cosmetic LiquidsTS EN ISO 18415 Detection of Transient Organisms in ToiletriesTS EN ISO 21148 Enumeration of Microorganisms in Cosmetic ProductsUSP <1227> Validation of Microbial Recovery in Cosmetic ProductsUSP <1231> Water Quality for Microbiological Control in Cosmetic ProductionUSP <2021> Microbial Control of Nutraceutical-Cosmetic HybridsUSP <2022> Evaluation of Cosmetic Quality Control ProtocolsUSP <51> Antimicrobial Effectiveness Testing (Preservative Challenge Test)USP <61> Microbial Enumeration Testing for Non-Sterile CosmeticsUSP <62> Testing for Specified Microorganisms in CosmeticsUSP <791> pH Control and Microbial Growth AssessmentWHO Guidelines for the Microbiological Control of Herbal Cosmetics

Hygiene Control of Cosmetic Containers and Closures: TS EN 12353 Testing Services

Introduction

In the cosmetics industry, ensuring the safety and efficacy of products is crucial for building customer trust and confidence. One critical aspect of product safety is the hygiene control of cosmetic containers and closures, which is governed by the European standard TS EN 12353. In this article, we will provide a comprehensive guide to understanding the importance, requirements, and benefits of TS EN 12353 testing services, as offered by Eurolab.

Standard-Related Information

TS EN 12353 is a European Standard that provides guidelines for the hygiene control of cosmetic containers and closures. It ensures that these products meet the required safety standards, which are essential for protecting consumers from potential health risks.

The standard specifies the requirements for:

1. Materials: TS EN 12353 sets forth specific material requirements for containers and closures to ensure they do not release harmful substances into the product.

2. Design and construction: The standard outlines design and construction requirements for containers and closures, including aspects such as labeling, sealing, and closure mechanisms.

3. Testing: TS EN 12353 describes the testing procedures necessary to verify compliance with the standard.

International and National Standards

TS EN 12353 is a harmonized standard that aligns with international standards, ensuring seamless trade and regulatory compliance across borders. The following national standards are equivalent to TS EN 12353:

  • ASTM D5989 (USA)
  • ISO 10993-15 (International)
  • TSE 11881 (Turkey)
  • Standard Development Organizations

    Standards development organizations play a crucial role in shaping industry practices and ensuring product safety. Eurolab, as an accredited testing laboratory, collaborates with standard development organizations to stay up-to-date on the latest standards and guidelines.

    Evolution of Standards

    Standard Numbers and Scope

    TS EN 12353:2017 A1:2020

  • Title: Hygiene control of cosmetic containers and closures
  • Number of pages: 12
  • Published date: December 2017, revised July 2020
  • Compliance Requirements for Different Industries

    TS EN 12353 is a critical testing service for various industries, including:

  • Cosmetics manufacturers
  • Personal care product suppliers
  • Pharmaceutical companies (for packaging materials)
  • Food and beverage industry (for food contact materials)
  • Standard Requirements and Needs

    Why is TS EN 12353 Hygiene Control of Cosmetic Containers and Closures Testing Required?

    1. Business and Technical Reasons: Regulatory compliance, quality assurance, and customer safety are driving forces behind the need for this testing service.

    2. Consequences of Non-Compliance: Failure to comply with TS EN 12353 can result in product recalls, fines, and reputational damage.

    3. Risk Factors and Safety Implications: Cosmetic containers and closures can pose health risks if not designed or manufactured correctly.

    Competitive Advantages

    Performing TS EN 12353 testing provides numerous benefits, including:

    1. Enhanced Product Safety: Ensures consumer safety by verifying the hygiene control of cosmetic containers and closures.

    2. Compliance with Regulations: Demonstrates adherence to national and international standards, facilitating trade and market access.

    3. Competitive Advantage: Differentiates products from competitors and showcases a commitment to quality and safety.

    Cost-Benefit Analysis

    The costs associated with TS EN 12353 testing are minimal compared to the benefits of ensuring product safety, regulatory compliance, and enhanced customer trust.

    Test Conditions and Methodology

    TS EN 12353 testing involves a series of laboratory tests designed to verify the hygiene control of cosmetic containers and closures. The following steps outline the test methodology:

    1. Sample Preparation: Selecting suitable samples for testing.

    2. Testing Parameters: Conducting various tests, including chemical analysis, biological evaluation, and physical assessment.

    3. Measurement and Analysis Methods: Utilizing advanced analytical techniques to assess sample properties.

    Test Reporting and Documentation

    Eurolab provides detailed test reports that comply with international standards and regulatory requirements. The report includes:

    1. Summary of Test Results: Verifies compliance with TS EN 12353.

    2. Interpretation of Results: Provides an expert analysis of test results, including recommendations for improvement.

    3. Certification and Accreditation Details: Demonstrates Eurolabs accreditation to ISO/IEC 17025.

    Why This Test Should be Performed

    TS EN 12353 testing provides numerous benefits, including:

    1. Risk Assessment and Mitigation: Identifies potential health risks associated with cosmetic containers and closures.

    2. Quality Assurance and Compliance Benefits: Ensures compliance with national and international standards, facilitating trade and market access.

    3. Competitive Advantage: Differentiates products from competitors and showcases a commitment to quality and safety.

    Conclusion

    TS EN 12353 is an essential testing service for ensuring the hygiene control of cosmetic containers and closures. By understanding the importance, requirements, and benefits of this standard, industries can ensure product safety, regulatory compliance, and enhanced customer trust. Eurolabs TS EN 12353 testing services provide a comprehensive solution to meet the evolving needs of the cosmetics industry.

    References

  • European Standard EN 12353:2017 A1:2020
  • ASTM D5989 (USA)
  • ISO 10993-15 (International)
  • TSE 11881 (Turkey)
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