August 15, 2022
HRP-502c Institutional Consent Language has been revised related to confidentiality language and ceded study consent documents.
May 18, 2022
Starting this month, the IRB will start requesting PIs use a slightly different ClinicalTrials.gov statement for their non-ACT studies registering with ClinicalTrials.gov.
November 17, 2021
The Investigator Manual has been updated to describe consent guidelines for special populations that may require alternative consent processes.