NBN EN ISO 11607-2 : 2006 AMD 1 2014
Current
The latest, up-to-date edition.
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES (ISO 11607-2:2006/AMD 1:2014)
12-01-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
4.1 Quality systems
4.2 Sampling
4.3 Test methods
4.4 Documentation
5 Validation of packaging processes
5.1 General
5.2 Installation qualification (IQ)
5.3 Operational qualification (OQ)
5.4 Performance qualification (PQ)
5.5 Formal approval of the process validation
5.6 Process control and monitoring
5.7 Process changes and revalidation
6 Packaging system assembly
7 Use of reusable sterile barrier systems
8 Sterile fluid-path packaging
Annex A (informative) - Process development
Annex ZA (informative) - Relationship between this International
Standard and the Essential Requirements
of EU Directive 93/42/EEC on medical
devices
Bibliography
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