A data/specimen transfer agreement allows a researcher to share data and/or specimens with a collaborator (a person or entity not associated with the study or the researcher’s institution).
The IRB will review direct advertisements (per FDA guidance, “advertising that is intended to be seen or heard by prospective subjects to solicit their participation in a study”) for each research
A Principal Investigator (PI) is the individual responsible for carrying out plans approved by an IRB. A Faculty Advisor (FA) is the individual responsible for oversight of research conducted by