| Institutional Review Boards for Clinical Drug Trials Pharmaceuticals_and_biotechnology > Clinical trials > Institutional Review Boards for Clinical Drug Trials |  |
Research firm providing Institutional Review Board (IRB) services as well as consulting in clinical trials development.
Guidance on reporting adverse events to Institutional Review Boards for NIH-supported multi-center clinical trials.
IRB for the University of Utah for research with human subjects.
Center for Drug Evaluation and Research, information on IRB's and their roles.
Resources of information, handbooks and guidelines from University of Illinois.
Nonprofit, institutional review board that provides contract services for the regulatory review of clinical trials.
A committee designated by an institution to review, to approve the initiation of, and to conduct periodic review of research involving human subjects, at the University of Maryland.
Electronic discussion of ethical, regulatory and policy concerns with human subjects research.
Independent Review Board meets weekly for the thorough ethical review of clinical research studies. The IRB staff strives to process resulting documents within 72 hours of each meeting.
From the Office for Human Research Protections.
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