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비즈니스 · 2000. 10. 6.1 분 읽기
Regulations Requiring Manufacturers to Assess the Safety and Effectiveness of New Drugs and Biological Products in Pediatric Patients; Technical Amendment
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요약
The Food and Drug Administration (FDA) is amending the biologics regulations to reincorporate a regulation that was inadvertently omitted. This action is being taken to improve the accuracy of the regulations.
원본 출처 언어: Federal Register — Food and Drug Administration원문 발표 열기 →