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BS EN ISO 11607-2:2020+A11:2022

$142.49

Packaging for terminally sterilized medical devices – Validation requirements for forming, sealing and assembly processes

Published By Publication Date Number of Pages
BSI 2022 32
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PDF Catalog

PDF Pages PDF Title
2 National foreword
6 European foreword
Anchor 5
European foreword to amendment A11
8 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
11 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
13 Annex ZC (informative) Relationship between this European Standard and the essential requirements of Directive 98/79/EC [OJ L 331] aimed to be covered
16 Foreword
17 Introduction
19 1 Scope
2 Normative references
3 Terms and definitions
23 4 General requirements
4.1 Quality systems
24 4.2 Risk management
4.3 Sampling
4.4 Test methods
4.5 Documentation
25 5 Validation of packaging processes
5.1 General
5.2 Installation qualification
26 5.3 Operational qualification
27 5.4 Performance qualification
5.5 Formal approval of the process validation
28 5.6 Process control and monitoring
5.7 Process changes and revalidation
6 Assembly
29 7 Use of reusable sterile barrier systems
8 Sterile fluid-path packaging
30 Annex A (informative) Process development
31 Bibliography
BS EN ISO 11607-2:2020+A11:2022
$142.49