Medical Device Single Audit Program

Friday, 27 October 2017 by

International Medical Device Regulators Forum International Coalition Pilot Program

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I. Background The  International Medical Device Regulators Forum (IMDRF) recognizes the value in developing a global approach to auditing and monitoring the manufacturing of medical devices to ensure safe medical devices.  The IMDRF, at its inaugural meeting in Singapore in 2012, identified a Work Group to develop specific documents for advancing the concept of the

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