Comprehensive Guide to USP <62> Tests for Specified Microorganisms in Contact Materials Laboratory Testing Service
Provided by Eurolab
The United States Pharmacopeia (USP) <62> tests for specified microorganisms in contact materials are a critical component of ensuring the safety and efficacy of medical devices, equipment, and other products that come into contact with patients or users. These tests are designed to detect the presence of microorganisms such as bacteria, viruses, fungi, and yeasts on the surface of these products.
Relevant Standards
The following standards govern USP <62> Tests for Specified Microorganisms in Contact Materials:
USP <62>: Tests for Specified Microorganisms in Contact Materials ISO 11737-1:2009: Sterilization of medical devices Microbiological removal testing of integrated thermometers and temperature-sensing devices, Part 1: General requirements ASTM F2096-13: Standard Guide for Selecting and Testing Medical Device Materials EN ISO 11737-2:2019: Sterilization of medical devices Microbiological removal testing of integrated thermometers and temperature-sensing devices, Part 2: Biological indication of sterilization by ionizing radiation Legal and Regulatory Framework
The legal and regulatory framework surrounding USP <62> Tests for Specified Microorganisms in Contact Materials is governed by various national and international regulations. These include:
US FDA: Medical Device Regulation EU MDR: Medical Device Regulation (2017/745/EU) ISO 13485:2016: Medical devices Quality management systems Requirements for regulatory purposes International and National Standards
The following international and national standards apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
USP <62>: Tests for Specified Microorganisms in Contact Materials ISO 11737-1:2009: Sterilization of medical devices Microbiological removal testing of integrated thermometers and temperature-sensing devices, Part 1: General requirements ASTM F2096-13: Standard Guide for Selecting and Testing Medical Device Materials EN ISO 11737-2:2019: Sterilization of medical devices Microbiological removal testing of integrated thermometers and temperature-sensing devices, Part 2: Biological indication of sterilization by ionizing radiation Standard Development Organizations
The following standard development organizations are responsible for developing and maintaining standards related to USP <62> Tests for Specified Microorganisms in Contact Materials:
US Pharmacopeial Convention (USP) International Organization for Standardization (ISO) American Society for Testing and Materials (ASTM) Standard Evolution and Updates
Standards related to USP <62> Tests for Specified Microorganisms in Contact Materials are subject to periodic review and update. This ensures that the standards remain relevant and effective in ensuring product safety and efficacy.
Specific Standard Numbers and Scope
The following specific standard numbers and scope apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
USP <62>: Tests for Specified Microorganisms in Contact Materials Scope: This test is intended to detect the presence of microorganisms on the surface of medical devices, equipment, and other products that come into contact with patients or users.
ISO 11737-1:2009: Sterilization of medical devices Microbiological removal testing of integrated thermometers and temperature-sensing devices, Part 1: General requirements Scope: This standard provides general requirements for the sterilization of medical devices using microbiological removal testing.
ASTM F2096-13: Standard Guide for Selecting and Testing Medical Device Materials Scope: This guide provides recommendations for selecting and testing medical device materials to ensure their safety and efficacy.
Industry-Specific Compliance Requirements
Compliance requirements for industries that require USP <62> Tests for Specified Microorganisms in Contact Materials include:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.USP <62> Tests for Specified Microorganisms in Contact Materials are required to ensure product safety and efficacy. This test is essential for industries that require compliance with regulatory requirements, such as medical devices and pharmaceuticals.
Business and Technical Reasons for Conducting USP <62> Tests for Specified Microorganisms in Contact Materials
The business and technical reasons for conducting USP <62> Tests for Specified Microorganisms in Contact Materials include:
Ensuring Product Safety: This test detects the presence of microorganisms on the surface of medical devices, equipment, and other products that come into contact with patients or users. Compliance with Regulatory Requirements: Manufacturers must comply with regulations such as the EU MDR and FDAs Medical Device Regulation to ensure product safety and efficacy. Ensuring Product Efficacy: This test ensures that medical devices, equipment, and other products function as intended. Industry-Specific Compliance Requirements
Compliance requirements for industries that require USP <62> Tests for Specified Microorganisms in Contact Materials include:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP. Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.Industry-Specific Requirements for USP <62> Tests for Specified Microorganisms in Contact Materials
The following industry-specific requirements apply to USP <62> Tests for Specified Microorganisms in Contact Materials:
Medical Devices: Manufacturers of medical devices must comply with regulations such as the EU MDR and FDAs Medical Device Regulation. Pharmaceuticals: Pharmaceutical manufacturers must comply with regulations such as the EU GMP and FDAs cGMP.
