As we near the end of 2015, the pilot phase of the International Medical Device Regulators Forum’s (IMDRF) Medical Device Single Audit Program (MDSAP) is approaching its third and final year. In this article, we’ll provide a review of the pilot study’s progress since its inception two years ago, and a preview of what’s ahead for single audits for medical device manufacturers. For more information on IMDRF’s Medical Device Single Audit Program, please click here.

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