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NS EN 13612 : 1ED 2002

Current
Current

The latest, up-to-date edition.

PERFORMANCE EVALUATION OF IN VITRO DIAGNOSTIC MEDICAL DEVICES
Published date

01-12-2013

Foreword
Introduction
1 Scope
2 Terms and definitions
3 General requirements for the performance evaluation
  3.1 Responsibilities and resources
  3.2 Documentation
  3.3 Final assessment and review
4 Organisation of a performance evaluation study
  4.1 Preconditions
  4.2 Evaluation plan
  4.3 Sites and resources
  4.4 Basic design information
  4.5 Experimental design
  4.6 Performance study records
  4.7 Observations and unexpected outcomes
  4.8 Evaluation report
5 Modifications during the performance evaluation study
6 Re-evaluation
7 Protection and safety of probands
Annex ZA (informative) Clauses of this European Standard
         addressing essential requirements or other
         provisions of EU Directives
Bibliography

Specifies performance evaluation of in vitro diagnostic medical devices (IVD MDs) including IVD MDs for self-testing. Also defines the responsibilities and general requirements for the planning, conduct, assessment and documentation of a performance evaluation study by the manufacturer.

DocumentType
Standard
PublisherName
Norwegian Standards (Norges Standardiseringsforbund)
Status
Current

Standards Relationship
EN 13612:2002/AC:2002 Identical
UNE-EN 13612:2002 Identical
UNI EN 13612 : 2002 Identical
DIN EN 13612:2002-08 Identical
BS EN 13612:2002 Identical

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