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jan 1, 2007 - Food and Drug Administration Amendments Act of 2007

Description:

Specifically authorized FDA to require manufacturers post-marketing clinical studies to monitor for risks infected during the pre-market approval process
Also required REMS programs where necessary. What is a REMS program?

Added to timeline:

Pharmacy Law Timeline

ByRachel Collins
21 Feb 2023
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Date:

jan 1, 2007
Now
~ 18 years ago
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