ClinicalTrials.gov: Essentials for Academic Medical Centers, Panel 3

Date/Time: Jul 30, 2026, 12:00 PM to Jul 30, 2026, 01:00 PM

Location: Virtual

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About this Event (Hosted by CDER SBIA)

This virtual training is designed to help staff at academic medical centers meet the federal requirements for registering clinical studies and reporting results on ClinicalTrials.gov. Specialists from the Center for Drug Evaluation and Research (CDER), Center for Devices and Radiological Health (CDRH), Office of Clinical Policy (OCLP) and the Center for Biologics Evaluation and Research (CBER) within the U.S. Food and Drug Administration (FDA), and the National Library of Medicine (NLM) within the National Institutes of Health (NIH) will address frequently asked questions regarding regulatory obligations and the ClinicalTrials.gov Protocol Registration and Results System (PRS).

This training begins with a required, pre-recorded video that you can complete at your own pace prior to registering for the live panel session that best fits your schedule or area of interest. Upon completion of the pre-recorded training, we encourage you to submit questions for our expert panel to address during the live sessions. You can submit your questions by emailing ClinicalTrials.govAMCTraining@fda.hhs.gov or by including them when you register for a live session. The panel will use your questions to guide the discussion and provide relevant, practical answers. The live panel sessions are designed to build upon the information presented in the on-demand video.

These sessions will help you and your team understand when and how to register and report clinical trial information to ClinicalTrials.gov and meet data transparency requirements. By completing the pre-recorded training and joining the live virtual panel, you will leave with practical information in order to share clinical trial information with the public accurately and on time.

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