Consentimento informado
Guia para comissões de análise institucionais, investigadores clínicos e promotores
Informed Consent - Guidance for IRBs, ClinicalInvestigators, and Sponsors
U.S. Department of Health and Human Services, Food and Drug Administration, Office of Clinical Policy, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research, Center for Devices and Radiological Health
Agosto 2023
U.S. Department of Health and Human Services, Food and Drug Administration, Office of Clinical Policy, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research, Center for Devices and Radiological Health
Agosto 2023
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