NBN EN 928 : 1996
Withdrawn
IN-VITRO-DIAGNOSTISCHE SYSTEMEN - LEIDRAAD VOOR DE TOEPASSING VAN EN 29001 EN EN 46001 EN VAN EN 29002 EN EN 46002 VOOR IN-VITRO-DIAGNOSTISCHE MEDISCHE HULPMIDDELEN
01-12-2013
12-01-2004
Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Guidance on quality system requirements
4.1 Management responsibility
4.2 Quality system
4.3 Contract review
4.4 Design control
4.5 Document control
4.6 Purchasing
4.7 Purchaser supplied product
4.8 Product identification and traceability
4.9 Process control
4.10 Inspection and testing
4.11 Inspection, measuring and test equipment
4.12 Inspection and test status
4.13 Control of nonconforming product
4.14 Corrective action
4.15 Handling, storage, packaging and delivery
4.16 Quality records
4.17 Internal quality audits
4.18 Training
4.19 Servicing
4.20 Statistical techniques
Annex A (informative) Bibliography
| DocumentType |
Standard
|
| PublisherName |
Belgian Standards
|
| Status |
Withdrawn
|
| Standards | Relationship |
| DIN EN 928:1995-12 | Identical |
| EN 928 : 1995 | Identical |
| I.S. EN 928:1996 | Identical |
| UNE-EN 928:1996 | Identical |
| BS EN 928:1996 | Identical |