BS EN 13612:2002

Foreword
Introduction
1 Scope
2 Terms and definitions
3 General requirements for the performance evaluation
4 Organisation of a performance evaluation study
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

Pertains to the performance evaluation of in vitro diagnostic medical devices (IVD MDs) including IVD MDs for self-testing.

This European Standard applies to the performance evaluation of in vitro diagnostic medical devices (IVD MDs) including IVD MDs for self-testing. It specifies the responsibilities and general requirements for the planning, conduct, assessment and documentation of a performance evaluation study by the manufacturer. It does not apply to specific evaluation plans for certain IVD MDs or a specific use. NOTE For a selection of publications on specific evaluation plans see Bibliography. Where a manufacturer maintains a quality system this standard addresses the compliance with \'design validation\' and \'design changes\' as described in EN ISO 9001, EN 46001 and EN 928 especially considering the nature and use of IVD MDs. In particular, this standard applies to IVD MDs to - show evidence to notified bodies and national authorities by results of a performance evaluation that the IVD MD performs as claimed by the manufacturer, - establish adequate performance evaluation data originating from appropriate studies or resulting from available literature, and to - satisfy the requirements of a quality system for design validation.