Bioethics Blogs

Unpacking OHRP’s and FDA’s Draft Guidance on IRB Meeting Minutes

In November 2015, the Department of Health and Human Services (DHHS) Office for Human Research Protections (OHRP) and the Food and Drug Administration (FDA) jointly released draft guidance for institutional review boards (IRBs) who oversee human subjects research under the FDA and/or DHHS regulations. This is the first time the agencies have jointly issued specific […]

The post Unpacking OHRP’s and FDA’s Draft Guidance on IRB Meeting Minutes appeared first on Ampersand.

The views, opinions and positions expressed by these authors and blogs are theirs and do not necessarily represent that of the Bioethics Research Library and Kennedy Institute of Ethics or Georgetown University.