The virtual training, ClinicalTrials.gov: Essentials for Academic Medical Centers, 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, you may register and submit your questions for any of the three upcoming live panel sessions via the links below:
- Panel One: Tuesday, July 14: 1:00 PM ET
- Panel Two: Wednesday, July 22: 1:00 PM ET
- Panel Three: Thursday, July 30: 1:00 PM ET