ON DEMAND EDUCATION FROM INDUSTRY SUBJECT MATTER EXPERTS

MDR Impact Outside of the EU

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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.

In This Video You'll Learn About...
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What Changes are Required for the Devices per MDR
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Heavy Hitters – Product Impact
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Heavy Hitters – Quality System Impact
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How Can I Prepare for the International Impact Now?
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Decision to Rationalize
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Managing the Supply Chain
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Take Action Early
 
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PRESENTED BY

SUSAN SPEICHER

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.

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