The University of Nevada, Reno IRB documents discussions, decisions, and findings from IRB meetings through its minutes; and for administrative, exempt, and expedited reviews, through documentation in ...

The guidance is intended to assist institutional review boards and institutions in developing written procedures. Whether an IRB has written procedures on the topics identified in the guidance may ...

Reports of noncompliance or protocol deviations must be submitted to the IRB within 48 hours of discovery. Please see this guidance document on how to submit reports. An "incident" should be submitted ...

When is IRB Approval Required? If your project involves "research" and "human subjects" as defined by 45 CFR 46, you must submit an application to the Case Western Reserve University Institutional ...

Primary members attend IRB meetings as voting members. Alternative members attend IRB meetings as voting members only when replacing a specified Primary member; when the specified Primary member is ...

Independent institutional review board Copernicus Group has announced CGIRB Connexus, a web portal for document management. The system integrates the management of electronic documents with a tracking ...

The US Food and Drug Administration (FDA) has joined forces with the Office for Human Research Protections (OHRP) to prepare draft guidance on how to record the activities of institutional review ...

Occasionally, researchers will need to submit their research to more than one research committee. This guidance addresses when submitting to the IBC and IRB is required. IRB and IBC review can be ...

Most Santa Clara University employees and students who plan to conduct research with human participants must obtain approval from the Santa Clara University Institutional Review Board (IRB) before ...

WIRB-Copernicus Group, the world’s leading provider of solutions that measurably improve the quality and efficiency of clinical research, announced that it is partnering with Veeva Systems Inc. to ...