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ISO 11737-3:2023PublishedSterilization of health care products — Microbiological methods — Part 3: Bacterial endotoxin testingISO 11737-2:2019PublishedSterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization processISO 11737-1:2018PublishedSterilization of health care products — Microbiological methods — Part 1: Determination of a population of microorganisms on productsISO/TS 20853:2026PublishedBiotechnology — Bioprocessing — General requirements for bacteriophage preparation for therapeutic useISO/TS 22456:2021PublishedSterilization of healthcare products — Microbiological methods— Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based productsISO/DIS 11737-1Under developmentSterilization of health care products — Microbiological methods — Part 1: Determination of a population of microorganisms on productsISO 11737-2:2009WithdrawnSterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization processISO 11737-1:2006WithdrawnSterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on productsISO 11737-3:2004WithdrawnSterilization of medical devices — Microbiological methods — Part 3: Guidance on evaluation and interpretation of bioburden dataISO 11737-2:1998WithdrawnSterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the validation of a sterilization processISO 11737-1:1995WithdrawnSterilization of medical devices — Microbiological methods — Part 1: Estimation of population of microorganisms on products