US, Canada expect Medical Device Single Audit Program draft guidelines this month
This article was originally published in Clinica
Executive Summary
The US Department of Commerce has released an annual work plan that outlines the ongoing efforts between the US and Canada to align their medical device regulations. Among the initiatives, the governments are working together on finalizing Medical Device Single Audit Program (MDSAP) guidances and draft versions of these are expected to be delivered in June.
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Global Pharma Guidance Tracker – March 2024
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