Pharmacovigilance – Code of Federal Regulation
eCFR :: 21 CFR 600.80 — Postmarketing reporting of adverse experiences. Title 21 —Food and DrugsChapter I —Food and Drug Administration, Department of Health and Human ServicesSubchapter F —BiologicsPart 600 —Biological Products: GeneralSubpart D —Reporting of Adverse ExperiencesSource: 59 FR 54042, Oct. 27, 1994, unless otherwise noted.Authority: 21 U.S.C. 321, 351, 352, 353, 355, 356c,…
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