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Information sheet guidance for institutional review boards and clinical investigators (use of investigational products when subjects enter a second institution)
Information sheet guidance for institutional review boards and clinical investigators (continuing review after study approval)
Information sheet guidance for institutional review boards and clinical investigators (sponsor - investigator - IRB interrelationship)
Information sheet guidance for institutional review boards and clinical investigators (exception from informed consent for studies conducted in emergency settings; regulatory language and excerpts from preamble)
Information sheet guidance for institutional review boards and clinical investigators (a guide to informed consent)
Information sheet guidance for institutional review boards and clinical investigators (charging for investigational products)
Information sheet guidance for institutional review boards and clinical investigators (non-local IRB review)
Information sheet guidance for institutional review boards and clinical investigators (recruiting study subjects)
Information sheet guidance for institutional review boards and clinical investigators (cooperative research)
Information sheet guidance for institutional review boards and clinical investigators (screening tests prior to study enrollment)
Information sheet guidance for institutional review boards and clinical investigators (acceptance of foreign clinical studies)
Information sheet guidance for institutional review boards and clinical investigators (frequently asked questions)
Information sheet guidance for institutional review boards and clinical investigators ("off-label" and investigational use of marketed drugs, biologics, and medical devices)
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Information sheet
ID:
3444655
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