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비즈니스 · 2003. 6. 18.1 분 읽기
Safety Reporting Requirements for Human Drug and Biological Products; Extension of Comment Period
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요약
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.
원본 출처 언어: Federal Register — Food and Drug Administration원문 발표 열기 →