The NINDS Topics in Clinical Research Seminar Series Presents, ClinicalTrials.gov: Overview of Registration and Results Reporting Requirements
Please log on for the next Topics in Clinical Research where we welcome Anna M. Fine, PharmD, MS, Acting Director of ClinicalTrials.gov, National Library of Medicine, NIH as she addresses the importance of and requirements for registering and submitting summary results information for NIH funded studies.
Attendees will hear directly from ClinicalTrials.gov regarding key reasons to register and report results of clinical trials, share tips, and provide updates on efforts to modernize the system… with Q&A to follow!
Dr. Anna M. Fine, PharmD, MS joined the National Library of Medicine, NIH in 2018 and is Acting Director of ClinicalTrials.gov. She leads the scientific, policy, regulatory, and outreach activities related to the operation of ClinicalTrials.gov, including the modernization initiative. Her previous experience includes over a decade of service in stakeholder engagement, adverse drug event reporting, and supervisory roles at the U.S. Food and Drug Administration.