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Negócios · 27/12/20211 min de leitura
Pathology Peer Review in Nonclinical Toxicology Studies: Questions and Answers; Guidance for Industry; Availability
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Resumo
The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry entitled "Pathology Peer Review in Nonclinical Toxicology Studies: Questions and Answers." This guidance represents FDA's current thinking on the management and conduct of pathology peer review performed during good laboratory practice (GLP)-compliant toxicology studies. This guidance finalizes the draft guidance "Pathology Peer Review in Nonclinical Toxicology Studies: Questions and Answers" issued on September 30, 2019. This revision includes editorial changes to improve the clarity of the document.
Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →