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Science / Pharmaceutical sciences / Design of experiments / Medical ethics / Pharmaceutical industry / Institutional review board / Clinical trial / Informed consent / Food and Drug Administration / Pharmacology / Research / Clinical research


Human Research Subject Protection and Institutional Review Boards (IRB) Standard Operating Policies and Procedures (SOPP) Office of Regulatory Research Compliance
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Document Date: 2014-07-08 13:36:46

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City

Washington / D.C. / /

Facility

Howard University / THE NATIONAL CANCER INSTITUTE / /

MedicalTreatment

Gene Therapy / /

Organization

INSTITUTIONAL BIOLOGICAL SAFETY COMMITTEE / Department of Health and Human Services / NATIONAL CANCER INSTITUTE / Howard University / HUMAN RESEARCH SUBJECT PROTECTION AND INSTITUTIONAL REVIEW BOARD / OFFICE of REGULATORY RESEARCH COMPLIANCE / National Institute of Health / INSTITUTIONAL REVIEW BOARD / Food and Drug Administration / /

Position

INVESTIGATOR / /

ProvinceOrState

Washington / /

Technology

4.2 Protocol / 37 8.5 PROTOCOL / 5.6 Gene Transfer/Gene Therapy Protocols / PREVIOUSLY APPROVED PROTOCOL / /

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