An NIH-hosted workshop for FDA, OHRP, IRBs, and Investigators
Location:
Neuroscience Center (NSC) Building
6001 Executive Blvd,
Conference Room 1131 35/45/55
Rockville, MD 20852
The Office of Emergency Care Research will be sponsoring an in person (only) workshop based on case presentations of clinical trials that require Exemption from Informed Consent (EFIC) and the challenge of consent from those who are critically ill. Representatives from the Food and Drug Administration (FDA), the Department of Defense (DOD), the National Institutes of Health (NIH), members of academic and commercial Institutional Review Boards (IRBs), representatives from StrokeNet, the LITES, and the SIREN network, and members of the wider emergency care research community will all be in attendance.
EFIC Workshop Deck Summary(pdf, 9700 KB)