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 U.S. Food and Drug Administration (FDA) and 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 any or all of the live panel sessions. Upon completion of the pre-recorded training, you can submit any questions you have about ClinicalTrials.gov registration and reporting via the registration process to attend a live virtual session with a panel of experts. 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.