Бизнес · 07.07.20111 мин чтения
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Draft Guidance for Industry, Third Parties and Food and Drug Administration Staff; Medical Device ISO 13485:2003 Voluntary Audit Report Submission Program
Локальный автоматический перевод · Язык оригинального источника
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The Food and Drug Administration (FDA) is announcing that a