{"id":411144,"date":"2024-10-20T05:43:47","date_gmt":"2024-10-20T05:43:47","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-11607-12020a112022\/"},"modified":"2024-10-26T10:34:40","modified_gmt":"2024-10-26T10:34:40","slug":"bs-en-iso-11607-12020a112022","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-11607-12020a112022\/","title":{"rendered":"BS EN ISO 11607-1:2020+A11:2022"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
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2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
3<\/td>\n | Blank Page <\/td>\n<\/tr>\n | ||||||
4<\/td>\n | Blank Page <\/td>\n<\/tr>\n | ||||||
5<\/td>\n | Blank Page <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Annex ZA (informative)Relationship between this European Standard and the essential requirements of Directive 93\/42\/EEC [OJ L 169] (as amended) aimed to be covered <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | Annex ZB (informative)Relationship between this European Standard and the essential requirements of Directive 90\/385\/EEC [OJ L 189] (as amended) aimed to be covered <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | Annex ZC (informative)Relationship between this European Standard and the essential requirements of Directive 98\/79\/EC [OJ L 331] (as amended) aimed to be covered <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 4 General requirements 4.1 Quality systems 4.2 Risk management 4.3 Sampling 4.4 Test methods <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 4.5 Documentation 5 Materials, preformed sterile barrier systems and sterile barrier systems 5.1 General requirements <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | 5.2 Microbial barrier properties <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | 5.3 Compatibility with the sterilization process 5.4 Labelling system 5.5 Storage and transport of materials and preformed sterile barrier systems <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | 6 Design and development for packaging systems 6.1 General 6.2 Design <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | 7 Usability evaluation for aseptic presentation <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | 8 Packaging system performance and stability 8.1 General 8.2 Packaging system performance testing <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | 8.3 Stability testing 9 Packaging system validation and changes <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | 10 Inspection immediately prior to aseptic presentation 11 Information to be provided <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | Annex A (informative) Guidance on medical packaging <\/td>\n<\/tr>\n | ||||||
38<\/td>\n | Annex B (informative) Standardized test methods, guides and procedures that can be used to demonstrate conformity with the requirements of this document <\/td>\n<\/tr>\n | ||||||
49<\/td>\n | Annex C (normative) Test method for resistance of impermeable materials to the passage of air <\/td>\n<\/tr>\n | ||||||
50<\/td>\n | Annex D (informative) Environmental aspects <\/td>\n<\/tr>\n | ||||||
51<\/td>\n | Annex E (informative) Draft guidance on ways to differentiate a sterile barrier system from protective packaging <\/td>\n<\/tr>\n | ||||||
56<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Packaging for terminally sterilized medical devices – Requirements for materials, sterile barrier systems and packaging systems<\/b><\/p>\n |