Welcome to the AdvaMed Events & Education community! No matter your sector or stage of your career, AdvaMed has relevant and educational events to help you deepen your knowledge. Please explore our 2023 Events & Education programs below. We hope you find these materials helpful, and we encourage you to sign up to be the first to learn more about events like this in the future.

Webinar Recordings

Medtech Coverage, Coding and Reimbursement 101 and 201 Workshops

Learn the basic principles of how medical technologies are covered and paid by insurers, the challenges medtech companies face and strategies they can use to achieve positive outcomes for coverage and appropriate reimbursement during our online Medtech Coverage, Coding and Reimbursement 101 and 201 Workshops.

101 Workshop

The 101 Workshop will discuss the “three-legged stool” of payment—coding, coverage, and reimbursement—as well as reviewing market access opportunities for novel technologies through both existing Medicare payment pathways and proposals to streamline Medicare policies in the future. Preview the 101 Workshop agenda.

201 Workshop

The 201 Workshop will focus on special topics in reimbursement, including: how diagnostic tests are paid by Medicare; challenges in coverage pathways for digital technologies; and demonstrating value of medical technologies and data and evidence to be covered by public and private payers. Preview the 201 Workshop agenda.

2023 Medical Device Submissions Workshops: 510(k) and De Novo, IDE, PMA

Join us in May for our online Medical Device Submissions Workshops, including: 510(k) and De Novo, Investigational Device Exemption (IDE), and Premarket Approval (PMA) Submissions. These workshops are the ideal introductory program for professionals who are new to medical device regulatory affairs looking for an unparalleled opportunity to learn more about regulatory requirements for bringing products to market.

510(k) and De Novo Submissions Workshop

Gain strategies for assembling and streamlining effective 510(k) and De Novo submissions and obtain insight into FDA’s perspective on the 510(k) and De Novo review process during this in-depth workshop. Preview the 510(k) and De Novo agenda.

Investigational Device Exemption (IDE)

FDA and industry experts will share the guidelines governing when an investigational device exemption is required. Experts will share tips for making the best use of pre-submission meetings, break down the components of an IDE submission, and more. Preview the IDE agenda.

Premarket Approval (PMA)

This workshop will walk you through the practical steps of filing a PMA and offer you actionable tips on how to best navigate the PMA submission process. Required steps, best practices and preparation for inspection will be covered throughout this workshop. Preview the PMA agenda.