Part 2: Individual Participant Data Sharing Plans: What, Why, and How to Write One
ClinicalTrials.gov requirements and publisher expectations are changing the way studies are designed and publicized. Policies encouraging transparency and data sharing affect trial registration, updates, results reporting, and informed consent. Even if you have assistance with your ClinicalTrials.gov registration, you will save time and energy from grant application through the registration process if you understand ClinicalTrials.gov terminology and data sharing expectations.
Presentations, group exercises, and discussions with regulatory and data-sharing specialists will help participants learn how to meet these requirements while strengthening scientific practices.
This session will be held online, and the organizers will be in touch with more information after you register.
Part 1: Outcome Measures – Why Plain Language Matters in the Age of Transparency will take place on Tuesday, October 15, 2024, and requires a separate registration.
**Our aim is to provide an outstanding experience for all attendees. If you require reasonable accommodations to attend this workshop, please contact the organizer at least two weeks in advance of the event.