{"id":279092,"date":"2024-10-19T18:49:24","date_gmt":"2024-10-19T18:49:24","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-11737-22009\/"},"modified":"2024-10-25T15:23:09","modified_gmt":"2024-10-25T15:23:09","slug":"bs-en-iso-11737-22009","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-11737-22009\/","title":{"rendered":"BS EN ISO 11737-2:2009"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
12<\/td>\n | Scope Normative references Terms and definitions <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | Quality management system elements Documentation Management responsibility <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | Product realization Measurement, analysis and improvement Selection of product General Sample item portion (SIP) <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | Packaging of product and sample item portions Methods for performing tests of sterility <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | Assessment of method for performing tests of sterility Maintenance of the method for performing tests of sterility <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Sterilization of medical devices. Microbiological methods – Tests of sterility performed in the definition, validation and maintenance of a sterilization process<\/b><\/p>\n |