Researchers conducting clinical trials must comply with many rules and regulations. One of them is the requirement to register and report the results of an applicable clinical trials (ACT) in the ClinicalTrials.gov Protocol Registration and Results System (PRS). Researchers can also register clinical trials even if the clinical trial does not meet the definition of an applicable clinical trial.

This presentation will provide a roadmap for registration and results reporting to ClinicalTrials.gov:

• Purpose of registration and results reporting
• Record Basics - Steps to Posting a new Study Record on ClinicalTrials.gov
• Requirements for reporting results
• Consequences for non-compliance
• HawkIRB – Push to PRS feature
• PRS support, training, and assistance

NOTE: This is the same presentation as the September 2, 2021, ICTS Clinical Lecture Series.

Fall 2021 IRB presentations will be hybrid. You may attend in person or by Zoom. HSO staff will follow UI policy and CDC guidelines for wearing masks and other safety precautions. We ask attendees to do the same.

NOTE: IRB Presentations may be changed to virtual-only on short notice. We will notify everyone who is registered. Check this page for any updates.

Pre-registration is recommended.