Medical Device Submissions Series: 510(k) & De Novo Workshop
Join industry leaders for the in-depth 510(k) & De Novo Workshop for real-world case studies, submissions tips and best practices.
Events & Education
AdvaMed®’s Events and Education offer both members and nonmembers an opportunity to network and learn all year long, year after year.
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Medical Device Submissions Series: Investigational Device Exemption (IDE) Workshop
Our in-depth device submissions workshops will provide real-world case studies, tips and best practices directly from FDA and industry experts.
Medical Device Submissions Series: Premarket Approval (PMA) Workshop
Learn key PMA Submissions strategies to build a strong submissions, align with FDA expectations, and reduce delays.
2026 AdvaMed® CEO Summit
This event annually gathers leading medtech executives in an intimate setting to foster the spirit of community and collaboration.
MedTech Reimbursement Playbook
Learn the basic principles of how medical technologies are covered and paid by insurers and the challenges medtech companies face.
Tariffs: Navigating Customs Origins Requirements for tariffs, USMCA exemptions and beyond (Members Only)
Exclusive member webinar on tariffs, customs, USMCA rules of origin, and compliance strategies with expert Larry Friedman. Air Date April 4, 2025. Now On Demand!
Richardson Waiver Repeal: What it Means for Medtech
Sidley Austin, joined by HPA, led a program examining the impact of HHS repealing the so-called “Richardson Waiver”, including its history, how it could impact the activities of the U.S.…
Tariffs: Understanding the Nairobi Protocol and related Customs Procedures
Learn how the Nairobi Protocol may support duty-free access for medical devices under new tariffs.
Hear From Us
Sign up to receive emails highlighting our upcoming events, early registration savings, and engagement opportunities for the medical technology community.