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Zdrowie i gospodarka · 19/11/1998

Bioavailability and Bioequivalence Requirements; Abbreviated Applications; Proposed Revisions

The Food and Drug Administration (FDA) is proposing to revise its regulations on bioavailability and bioequivalence and on the content and format of an abbreviated application to reflect current FDA policy and to correct certain typographical and inadvertent errors. This action is intended to improve the accuracy and clarity of the regulations.

Source: Federal Register — Food and Drug AdministrationOpen original release →