Résumé
This part of EN ISO 14155 provides requirements for the preparation of a Clinical Investigation Plan (CIP) for the clinical investigation of medical devices. The compilation of a CIP in accordance with the requirements of this standard and adherence to it will help in optimising the scientific validity and reproducibility of the results of a clinical investigation.
This Standard does not apply to in vitro diagnostic medical devices.
Informations générales
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État actuel: AnnuléeDate de publication: 2003-05Stade: Annulation de la Norme internationale [95.99]
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Edition: 1
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Comité technique :ISO/TC 194ICS :11.100.20
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Cycle de vie
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Précédemment
AnnuléeISO 14155:1996
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Actuellement
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Révisée par
AnnuléeISO 14155:2011