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Shared Perspectives: Panel Discussion on What's on the Horizon for Diagnostics Regulation in the US and EU

April 6, 2021
Arnold & Porter Webinar
By Mahnu V. Davar Jacqueline Mulryne Alberto Gutierrez Sue Spencer

Our integrated and cross-functional medical device team present a three-part webinar series focused on various aspects of ITC litigation, including recent relevant trials, global privacy and data security concerns, and recent US and EU diagnostic regulatory challenges.

Alberto Gutierrez of NDA Partners LLC and Sue Spencer of Qserve Group UK join Arnold & Porter partners Mahnu Davar and Jackie Mulryne for the final webinar in this series, which will focus on cross-border diagnostic regulations. The program will provide an in-depth discussion on the key components and timelines for In Vitro Diagnostic Regulation (IVDR) and the VALID Act, as well as the impact of the these regulations on the clinical laboratory, digital health manufacturers and companion diagnostics industries. Join our expert panel as they unpack the key legal and regulatory issues relevant to your business.

Other Webinars in the Series

» Watch: The ITC and Its Application in Medical Device Litigation

» Watch: Protecting Data in Digital Health and Connected Devices

Meet the Speakers

Alberto Gutierrez
Partner, NDA Partners LLC
Sue Spencer
Head of In Vitro Diagnostics & Principal Consultant, Qserve Group UK
Mahnu V. Davar
Arnold & Porter
Jacqueline Mulryne
Arnold & Porter