SBIA Presents Live Panel One for ClinicalTrials.gov: Essentials for Academic Medical Centers Live Panel One: Tuesday, July 14: 1:00 PM ET

https://collaborationcqpub1.fda.gov/content/adobeconnect/213/7/en/events/event/private/164827404/284007766/event_landing.html?connect-session=breezbreezwg5fazv34hgme9xr&sco-id=284007767&_charset_=utf-8 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 the live panel session that best fits your schedule or area of interest. Upon completion of the pre-recorded training, you can submit any questions you have about ClinicalTrials.gov registration and reporting via the dedicated email account ClinicalTrials.govAMCTraining@fda.hhs.gov and also through 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. To get started, please complete the required pre-recorded training at your earliest convenience. Upon completion, you may register and submit your questions for any of the three upcoming live panel sessions via the links below: