
QMSR Transition: Legal and Audit Perspectives
Join Hogan Lovells experts to learn how the FDA is set to reshape the medical device regulatory landscape with the introduction of the QMSR.
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Join Hogan Lovells experts to learn how the FDA is set to reshape the medical device regulatory landscape with the introduction of the QMSR.

Join PRIA Healthcare to explore how a Patient Access Program can accelerate access and drive lasting medtech success.

Join The Mullings Group to learn strategies for hiring top performers and how medtech teams attract and retain talent.

Join industry leaders for the in-depth 510(k) & De Novo Workshop for real-world case studies, submissions tips and best practices.

Our in-depth device submissions workshops will provide real-world case studies, tips and best practices directly from FDA and industry experts.

Learn key PMA Submissions strategies to build a strong submissions, align with FDA expectations, and reduce delays.

Learn the basic principles of how medical technologies are covered and paid by insurers and the challenges medtech companies face.

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!

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.…

Learn how the Nairobi Protocol may support duty-free access for medical devices under new tariffs.
Sign up to receive emails highlighting our upcoming events, early registration savings, and engagement opportunities for the medical technology community.