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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.100 Laboratory medicine>11.100.10 In vitro diagnostic test systems>BS EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
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immediate downloadReleased: 2003-02-27
BS EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices

BS EN 13612:2002

Performance evaluation of in vitro diagnostic medical devices

CURRENCY
LANGUAGE
English
Standard number:BS EN 13612:2002
Pages:18
Released:2003-02-27
ISBN:0 580 39650 9
Status:Corrigendum
DESCRIPTION
This standard BS EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices is classified in these ICS categories:
  • 11.100.10 In vitro diagnostic test systems
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.
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