Colorado Senator: FDA Device Reforms Should Simplify Process

U.S. Senator Michael Bennet (D-Colorado) is urging the FDA to choose medical device regulatory reforms that will simplify manufacturing processes, according to a news release from Sen. Bennet.

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In a letter to the FDA, he also urged the agency to adopt successful approaches from other countries and consider private-public partnerships.

 

Earlier this week, the FDA announced a “Strategic Plan for Regulatory Science” initiative to foster innovation through better science.

 

Related Articles on FDA Medical Device Regulatory Reform:

New England Journal Agrees FDA Device Process Must be Overhauled

FDA Clarifies Device Approval Process

FDA Proposes Updating Device Reviews, Including for Joints, IOLs

 

 

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