Global Clinical Trial Disclosure and Data Transparency Conference

Learn about the latest requirements in clinical trial disclosure and data transparency, share best practices, and engage in in-depth discussions on hot topics.

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Session 4: ClinicalTrials.gov Updates and Modernization Highlights

Session Chair(s)

Suzanne Carlson, MA

Consultant

ABSD Associates, LLC, United States

Learn about ClinicalTrials.gov approach to Modernization and see a demonstration of the new PRS features. Members of the National Library of Medicine’s Modernization team will share an overview of the insights gained from user feedback, what issues will be addressed in the system, and what industry should know.

Learning Objective : At the conclusion of this session, participants should be able to:
List recent updates to ClinicalTrials.gov and convey the plans for and progress of modernization efforts

Describe features of the updated PRS modules

Summarize the upcoming changes for the ClinicalTrials.gov public site modernization

Speaker(s)

What’s New at ClinicalTrials.gov and Modernization Overview

Anna Fine, PharmD, MS

National Institutes of Health (NIH), United States

Interim Director for ClinicalTrials.gov

Modernization of PRS (Protocol Registration and Results System)

Stacey Arnold, PhD

National Institutes of Health (NIH), United States

Results Team Subject Matter Expert

Modernization of ClinicalTrials.gov

Christina Robinson, MA

National Institutes of Health (NIH), National Library of Medicine, United States

Technical Information Specialist

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