U.S. Can Improve Medical Device Approval Process While Ensuring Safety

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U.S. Can Improve Medical Device Approval Process While Ensuring Safety
The United States does not have to choose between the vitality of its medical device industry or the health of its people, U.S. Sen. Al Franken said in an interview at the Design of Medical Devices Conference hosted by the University of Minnesota. It is possible to improve both.

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Related Event:

Regulatory Information Management Conference
April 24-25 | Philadelphia

The Regulatory Information Management (RIM) Conference features business and technology tracks. The business track will focus on ways to obtain and manage regulatory information and the related organizational impact. The technology track will explore ways to create a business case for an RIM system, submission standards of regulatory information, manage the information, and identify key business drivers for establishing a global RIM system.

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Regulatory Affairs in the news...

In the news...

Regulatory Affairs

First 4 Things to do to Get FDA Approval
New drugs and medical devices cannot be sold to US customers before being approved by the FDA. Read more...

The following events focus on establishing effective regulatory information processes and strategies:

Regulatory Affairs Part I: The IND Phase
April 11-13 | Horsham, PA

European Regulatory Affairs
Begins April 20
Regulatory Information Management
April 24-25 | Philadelphia, PA