Tom Middleton

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Industry

Are You Ready for the MDSAP?

To streamline the oversight of manufacturers’ quality systems, and encourage improved product safety on a global scale, the International Medical Device Regulators Forum (IMDRF) has developed the Medical Device Single Audit Program (MDSAP).

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What's New

How AI is Changing the Regulation of Medical Devices

Averna Acquires Automated Test Solutions Provider ELCOM

Bureau Veritas Closes Mexico Acquisition

Product Insights: The Most Important Skill to Develop as a Compliance Professional

FDA Proposes Ban on Electrical Stimulation Devices

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