Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

SAN DIEGO, CA, UNITED STATES, September 12, 2025 / EINPresswire.com / -- PRP Labs, a national distributor of FDA-cleared regenerative medicine equipment, today announced the release of its Free PRP ...

The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating for the subject's right ...

Expedited studies are research projects that meet one of the categories under 46.110 and involve minimal risk. Full board studies are those the IRB determines does not fall under exempt or expedited ...

Prior to completing an application, you will need to satisfy training requirements. The Human Subject Research Orientation on Canvas will ultimately save you time in ...

Research by Johns Hopkins epidemiologists has confirmed what some have long suspected about consent forms required of clinical trial volunteers: They use language far too difficult for most people to ...

NOTE: The University IRB abides by information regarding the current position of the VHA Office of Research & Development’s (per email from Karen Jeans dated 01/03/14) related to use of Craigslist as ...