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FDA and industry experts are coming together to review the basics of 510(k) submissions. This unique opportunity will help you better understand the FDA perspective on 510(k) submissions, from proc... more
During this interactive workshop, FDA and industry experts will lead you through the regulatory and practical guidelines governing when an investigational device exemption (IDE) is required.... more
Completing the set of interactive submissions workshops, industry and FDA experts will lead you through the strategic considerations and practical steps of filing a Premarket Approval.
This annual conference brings together leading authorities from FDA, industry and academia to address the latest statistical trends and issues facing medtech organizations. This conference allows a... more
From products to consumers to regulation and new media—we’re gathering industry practitioners to take a deep dive into the opportunities and challenges of product advertising. This annual conferenc... more
From September 23–25, 2019, more than 3,300 of the world’s top medtech executives gathered in Boston, MA, for the leading event in our industry — The MedTech Conference. Join us again as we take To... more