Requirements for Medical Device Auditing Organizations for Regulatory Authority Recognition
Title:
Requirements for Medical Device Auditing
Organizations for Regulatory Authority Recognition
Origin/Publisher:
IMDRF
Content:
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 Single Audit Program (MDSAP). This document applies to Auditing Organizations that audit medical device manufacturers and
may perform other related functions.