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Imprese · 18/06/20031 min di lettura
Safety Reporting Requirements for Human Drug and Biological Products; Extension of Comment Period
Traduzione automatica locale · Lingua originale della fonte
Riepilogo
The Food and Drug Administration (FDA) is extending to October 14, 2003, the comment period for a proposed rule published in the Federal Register of March 14, 2003 (68 FR 12406). The proposed rule would amend the agency's pre- and postmarketing safety reporting regulations for human drug and biological products. The agency is taking this action in response to a request for more time to submit comments to FDA.
Lingua originale della fonte: Federal Register — Food and Drug AdministrationApri il comunicato originale →