Guidance for clinical investigators, sponsors, and IRBs [[electronic resource] ] : adverse event reporting to IRBs : improving human subject protection

• Pubblicazione: Rockville, MD : , : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner, , [2009]
• Descrizione fisica: 1 online resource (6 pages)
• Soggetto topico: Clinical trials - Reporting; Human experimentation in medicine; Institutional review boards (Medicine) - Government policy - United States
• Note generali: "Procedural".; "January 2009".
• Altri titoli varianti: Guidance for clinical investigators, sponsors, and IRBs
• Titolo autorizzato: Guidance for clinical investigators, sponsors, and IRBs
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910699066203321
• Lo trovi qui: Univ. Federico II