Informed Consent Posting of Clinical Trials
The 2018 Common Rule requires that for each clinical trial conducted or supported by a federal department or agency, one IRB-approved consent form for subject enrollment must be publicly posted on a federal website by the awardee or the federal department conducting the trial (applies to trials conducted or supported by the Department of Health and Human Services).
The Office for Human Research Protections (OHRP) provides general instruction on the informed consent posting requirement (45CFR46.116 (h))
Please review the OHRP website for information and guidance on Informed Consent Posting.
This document provides instructions on how, when, and where to post an informed consent.
Contact the School of Medicine Clinical Trials Office if you have questions regarding posting consent forms.