HRP’s Educational and Quality Improvement Program (EQUIP) and Health Compliance and Privacy Offices routinely review applicable studies to ensure compliance with ClinicalTrials.gov reporting requirements.
UPDATE: | Beginning in October 2022, email notifications will be sent to researchers when their ClinicalTrials.gov (CT.gov) record is out of compliance.
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For CT.gov questions or regulatory/institutional guidance, please contact equip@research.uci.edu or for technical questions or issues related to PROCoM, please contact ERA.