Requirements for Medical Device Auditing Organizations for Regulatory Authority Recognition

Titel:
Requirements for Medical Device Auditing Organizations for Regulatory Authority Recognition
Herkunft/Verlag:

IMDRF

Inhalt:
This is one document in a collection of documents produced by the International Medical Device Regulators Forum (IMDRF) intended to implement the concept of a Medical Device SingleAudit Program (MDSAP). This document applies to Auditing Organizations that audit medical device manufacturers and may perform other related functions.

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