Today at 1 p.m. CDER SBIA Webinar: Learn About ClinicalTrials.gov Modernization and How to Provide Input

Learn about ClinicalTrials.gov Modernization and how to Provide Input TODAY at 1:00 p.m. Eastern

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The National Library of Medicine (NLM) issued a Request for Information (RFI) to obtain stakeholder feedback on modernizing ClinicalTrials.gov. NLM is asking for your input on how to deliver an improved user experience on an updated platform that will accommodate growth and enhance efficiency. Creating a roadmap for modernization requires feedback from a wide array of stakeholders including sponsors and investigators who submit clinical trial information to the site on how to continue serving, balancing, and prioritizing their information needs. LEARNING OBJECTIVES Learn about the ClinicalTrials.gov modernization effort Understand how to submit comments that could shape enhancements to ClinicalTrials.gov List the three relevant topic areas where NLM is seeking input INTENDED AUDIENCE Study sponsors and investigators who use the Web-based submission system called the Protocol Registration and Results System (PRS) to ensure that their clinical studies are registered and have results reported on ClinicalTrials.gov. Researchers using ClinicalTrials.gov information to inform their work or to improve the clinical research enterprise (example, perform landscape analysis to understand what research has been completed or where gaps in research exist).   Clinical research coordinators who need to understand what information needs to be collected or reported to ClinicalTrials.gov.