A record of requests for the use of human subjects in research. May include application, sample consent forms for subjects, Review Committee's Disposition documentation, investigator's responses to the committee, application modifications, application annual reviews, final report, sponsor protocols, Adverse Event Reports, non-compliance documents, subject complaints, records requests, copies of Radiation Safety Committee Review, Certification of Review or documentation that certification was sent to funding agency, other supporting documentation, etc.
Official Copy: Human Subjects Division
Retention: 10 years after study termination
Disposition Method: Shred or Delete
Other Copy: Principal Investigator
Retention: 6 years after close of study, or 6 years after study termination if research is not grant/contract funded
Disposition Method: Shred or Delete