{"id":415583,"date":"2024-10-20T06:06:03","date_gmt":"2024-10-20T06:06:03","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-10993-22022\/"},"modified":"2024-10-26T11:20:32","modified_gmt":"2024-10-26T11:20:32","slug":"bs-en-iso-10993-22022","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-10993-22022\/","title":{"rendered":"BS EN ISO 10993-2:2022"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Annex ZA (informative)Relationship between this European Standard and the essential requirements of Directive 93\/42\/EEC [OJ L 169] aimed to be covered <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | Annex ZB (informative)Relationship between this European Standard and the essential requirements of Directive 90\/385\/EEC [OJ L 189] aimed to be covered <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | Annex ZC (informative)Relationship between this European standard and the General Safety and Performance Requirements of Regulation (EU) 2017\/745 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 \u200bScope 2 \u200bNormative references 3 \u200bTerms and definitions <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 4 \u200bRequirements 4.1 \u200bGeneral <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 4.2 \u200bJustification for animal tests <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 4.3 \u200bCompetence of personnel 4.4 \u200bPlanning and performance of animal tests 4.4.1 \u200bGeneral 4.4.2 \u200bRe-use <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 4.5 \u200bTest strategy \u2014 Sequence of in vitro and in vivo tests 4.6 \u200bAnimal care and accommodation 4.6.1 \u200bGeneral 4.6.2 \u200bRestraint 4.6.3 \u200bSurgical procedures <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 4.7 \u200bHumane end points 4.7.1 \u200bGeneral 4.7.2 \u200bEuthanasia 4.8 \u200bStudy documentation <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 4.9 \u200bValidity of test results and mutual acceptance of data <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | Annex A (informative) Rationale for the development of this document <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | Annex B (informative) Further suggestions for replacing, reducing and refining animal tests <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Biological evaluation of medical devices – Animal welfare requirements<\/b><\/p>\n |