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Sep 2023
55m 5s

#335: Accelerating SaMD Development in a...

Greenlight Guru + Medical Device Entrepreneurs
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Oct 15
#476: Part 2: FDA Guidance: What We Should Expect in 2027
In this episode of the Global Medical Device Podcast, host Etienne Nichols continues his conversation with regulatory consultant Michael Drues, Ph.D., to examine the FDA's Center for Devices and Radiological Health (CDRH) guidance document priorities for fiscal year 2027. The dis ... Show More
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#475: Part 1: Rethinking FDA Guidance: Why Non-Binding Documents Define Your Regulatory Strategy
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Building a medical device rarely follows the smooth, predictable trajectory presented in investor pitch decks. While regulatory consultants often default to "it depends," medical device teams require concrete figures regarding engineering hours, calendar timelines, and budget all ... Show More
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