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Session 2: ClinicalTrials.gov and EudraCT – An Update by NIH and EMA
Session Chair(s)
Robert Paarlberg, MS
Principal
Paarlberg & Associates LLC, United States
This session featuring representatives from NIH and EMA will provide an update on the requirements and status of ClinicalTrials.gov and EudraCT. The session will also have a panel for questions & answers.
Speaker(s)
Updates to the ClinicalTrials.gov Protocol Registration and Results System (PRS)
Nicholas C. Ide, MS
National Institutes of Health (NIH), United States
Chief Architect, ClinicalTrials.gov, National Library of Medicine
Updates to the ClinicalTrials.gov Protocol Registration and Results System (PRS)
Rebecca Williams, PharmD, MPH
Essex, Part of Emmes Group, United States
Senior Clinical Trials Subject Matter Expert
Updates to the EudraCT Database
Noemie Manent, PharmD
European Medicines Agency, Netherlands
TDA-CTT Operations Workstream Lead
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