{"id":279652,"date":"2024-10-19T18:52:49","date_gmt":"2024-10-19T18:52:49","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-19-30361785-dc\/"},"modified":"2024-10-25T15:26:54","modified_gmt":"2024-10-25T15:26:54","slug":"bsi-19-30361785-dc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-19-30361785-dc\/","title":{"rendered":"BSI 19\/30361785 DC"},"content":{"rendered":"
This document specifies the requirements for and provides guidance on the specification, selection, qualification, bio-decontamination, validation, operation and control of isolator systems related to aseptic processing of health care products and processing of cell based health care products.<\/p>\n
This document does not specify requirements for restricted access barrier systems (RABS).<\/p>\n
This document does not supersede or replace national regulatory requirements such as Good Manufacturing Practices (GMPs) and\/or compendia requirements that pertain in particular to national or regional jurisdictions.<\/p>\n
This document does not specify requirements for isolators used for sterility testing; however, some of the principles and information in this document could be applicable to this application.<\/p>\n
This International Standard does not define biosafety containment requirements.<\/p>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
7<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
10<\/td>\n | 4 Quality system elements 5 Basic principal of Isolator systems 5.1 General <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 5.2 Negative pressure isolators 6 Isolator System Specification 6.1 General <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 6.2 Risk management 6.2.1 General 6.2.2 Negative pressure isolators 6.3 User requirement specification <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | 7 Design of isolator systems 7.1 General 7.2 Materials of construction <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 7.3 Air-handling system 7.3.1 General 7.3.2 Air change rate 7.3.3 Airflow pattern 7.3.4 Temperature\/humidity 7.3.5 Particulate air specifications <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 7.3.6 Recirculation of air 7.3.7 Pressure differentials 7.4 Operator interface 7.4.1 Isolator gloves\/sleeves 7.4.2 Suits\/half-suits 7.4.3 Access to the isolator\/Transfer systems <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 7.4.4 Transfer ports 7.5 Ancillary isolator equipment 7.5.1 Portable and mobile equipment 7.6 Surrounding room classification <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 7.7 Process utilities 8 Validation 8.1 General 8.2 Design qualification 8.2.1 General 8.2.2 Product\/process application <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 8.2.3 Ergonomics 8.2.4 Cleaning <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 8.2.5 Bio-decontamination 8.2.6 Development and validation of bio-decontamination processes 8.2.7 Selection of bio-decontamination agent <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 8.2.8 Bio-decontamination agent generation and testing 8.2.9 Bio-decontamination parameters 8.2.10 Aeration and residue limits <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 8.2.11 Spore log reduction 8.2.12 Surface bio-decontamination of items 8.2.13 Development and validation of sterilization processes 8.3 Installation qualification 8.3.1 General <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 8.3.2 Installation 8.4 Operational qualification <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 8.5 Performance qualification 8.5.1 General 8.5.2 Cleaning <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 8.5.3 Bio-decontamination 8.5.4 Process simulation tests 8.6 \u200bReview and approval of validation 8.7 Requalification <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | 9 Routine monitoring and control 9.1 Procedures 9.2 System integrity 9.3 Bio-decontamination process monitoring 9.4 Environmental monitoring <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 9.5 Change control 9.6 Maintenance and calibration 10 Personnel training <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | Annex\u00a0A (informative) Transfer ports for portable and mobile equipment <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | Annex\u00a0B (informative) Isolator system \u2013 principal figure of term and flow diagram of air and material <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | Annex\u00a0C (informative) Isolator system \u2013 Critical surfaces in isolator system <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | Annex\u00a0ZA (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 | ||||||
36<\/td>\n | Annex\u00a0ZB (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 | ||||||
38<\/td>\n | Annex\u00a0ZC (informative) Relationship between this European Standard and the essential requirements of Directive 98\/79\/EC [OJ L 331] aimed to be covered <\/td>\n<\/tr>\n | ||||||
40<\/td>\n | Annex\u00a0ZD (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 | ||||||
43<\/td>\n | Annex\u00a0ZE (informative) Relationship between this European Standard and the General Safety and Performance Requirements of Regulation (EU) 2017\/746 aimed to be covered <\/td>\n<\/tr>\n | ||||||
46<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" BS EN ISO 13408-6. Aseptic processing of health care products – Part 6. Isolator systems<\/b><\/p>\n |