ON DEMAND EDUCATION FROM INDUSTRY SUBJECT MATTER EXPERTS
MDR Impact Outside of the EU
The goal of this presentation is to present a wide point of view addressing the MDR impact outside of the EU. This video discusses the required changes for devices per MDR, the kind of changes that will impact countries outside of the EU, and how to prepare for the international impact now. Susan Speicher will address techniques on how to save time and resources while implementing MDR changes throughout the world.
Director, Regulatory Affairs
* This presentation includes personal reviews of the presenters and information presented here may differ from actual regulatory requirements imposed by the health authorities.
* This presentation is limited to medical devices and the MDR, excluding in-vitro diagnosis devices and the IVDR.