On December 27, 2020, the President signed into law the “Consolidated Appropriations Act, 2021” (the “Act”). Included within this omnibus legislation are several provisions (in Division BB, Title III, Subtitle C) that affect the regulation of generic drugs and biosimilar medicines by the U.S. Food and Drug Administration (FDA).
The post Congress Enacts Amendments Affecting The Regulation Of Generic Drugs And Biosimilars appeared first on Life Sciences Perspectives.