Dave Padgett is a seasoned regulatory affairs professional and the owner of DPadgett Consulting, LLC, with over 25 years of experience in medical devices, IVDs, and tissue products. They have authored and submitted more than 100 FDA regulatory filings, including 510(k)s and PMAs, and have successfully navigated product registrations in multiple international markets. Currently, they provide strategic regulatory guidance and hands-on support for clients across various sectors, specializing in ISO certifications, post-market surveillance, and risk management. Dave is pursuing a Bachelor of Science in Biology at Florida State University.
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