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roducts;Quality assurance;Quality management;Raw materials;Reclamation;Release;Safety;Samples;Sampling methods;Selection;Solutions;Specification (approval);Sterile;Sterility;Sterilization (hygiene);Substances;Testing;Transfer;Transport;Treatment;Validation;Verification【摘要】: This part of ISO 11737 specifies requirements and provides guidance for the enumeration and microbialcharacterization of the population of viable microorganisms on or in a medical device, component, rawmaterial or package.This part of ISO 11737 does not specify requirements for the enumeration or identification of viral or protozoancontaminants.This part of ISO 11737 does not specify requirements for the microbiological monitoring of the environment inwhich medical devices are manufactured.【中国标准分类号】: C30【国际标准分类号】: 07_100_10;11_080_01【页数】: 35P;A4【正文语种】: 英语 | 欢迎光临 世界资料网论坛 (http://bbs.infoeach.com/) | Powered by Discuz! X2.5 |