{"id":291144,"date":"2024-10-19T19:45:56","date_gmt":"2024-10-19T19:45:56","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-en-iso-22442-12015\/"},"modified":"2024-10-25T16:47:25","modified_gmt":"2024-10-25T16:47:25","slug":"bs-en-iso-22442-12015","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-en-iso-22442-12015\/","title":{"rendered":"BS EN ISO 22442-1:2015"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
4<\/td>\n | European foreword <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Relationship between this European Standard and the Essential Requirements of EU Directive 93\/42\/EEC <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 1\tScope 2\tNormative references <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 3\tTerms and definitions <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 4\tRisk management process 4.1\tGeneral 4.2\tRisk analysis 4.2.1\tIdentification of qualitative and quantitative characteristics related to the safety of medical devices <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 4.2.2\tIdentification of hazards and hazardous situations <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 4.3\tRisk evaluation 4.4\tRisk control 4.4.1\tGeneral 4.4.2\tRisk control for viruses and TSE agents 4.4.3\tRisk control of other hazards <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 4.4.4\tResidual risk evaluation 4.5\tEvaluation of overall residual risk acceptability 4.5.1\tGeneral 4.5.2\tDocumentation <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 4.6\tProduction and post-production information system <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | Annex\u00a0A (informative) Guidance on the application of this part of ISO\u00a022442 <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | Annex\u00a0B (informative) Graphical representation of part of the risk management process for medical devices utilizing animal material <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | Annex\u00a0C (normative) Special requirements for some animal materials considering the risk management for TSE agents <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | Annex\u00a0D (informative) Information relevant to the management of TSE risk <\/td>\n<\/tr>\n | ||||||
36<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Medical devices utilizing animal tissues and their derivatives – Application of risk management<\/b><\/p>\n |