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  1. Clinical Trials and Human Subject Protection

Workshops and Meetings

Workshops and Meetings on Good Clinical Practice and Human Subject Protection

FDA Clinical Trial Requirements Regulations, Compliance, and GCP Conferences
The Society of Clinical Research Associates and FDA District Offices co-sponsor these conferences on FDA’s clinical trial and human subject protection regulations and requirements.

Clinical Investigator Training Course. A collaborative training course hosted by the U.S. Food and Drug Administration, Center for Drug Evaluation and Research’s (CDER’s) Office of Medical Policy (OMP), Small Business and Industry Assistance (SBIA) and University of Maryland’s Center of Excellence in Regulatory Science and Innovation (CERSI).

Office for Human Research Protections (OHRP) conferences. OHRP sponsors a variety of national and regional workshops about the roles and responsibilities of researchers, institutional review boards (IRBs), institutional officials, and others to promote the protection of human subjects in research. FDA participates in these programs to provide information about FDA’s regulatory requirements.

Other Meetings


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