Medical device companies are acutely familiar with FDA regulations and likely certified to, or working toward, a quality management standard like ISO 13485. Those that seek to expand business need to invest in one more pathway to success: the Medical Device Single Audit Program (MDSAP).
What is it and why should any medical device manufacturer care? Over the course of three days, we will introduce MDSAP, an optional compliance program that is altering the availability of markets for those that don’t jump aboard.
Join us for a peek at what companies need to do to conform.
Regulatory and quality personnel, as well as senior executives, of medical device manufacturers
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Another session may be scheduled if there is enough demand. Contact Gary Simon at ggsimon@buffalo.edu if interested.
