Is your organization reporting clinical-trial results on time?

Heavy fines are the penalty for failure to report study findings.

Read about research reporting problems with leading U.S. universities.


Protocol Registration and Results Summary Disclosure in ClinicalTrials.gov

CITI Program's Protocol Registration and Results Summary Disclosure in ClinicalTrials.gov course will provide a video-enhanced guide to compliance with the FDAAA Final Rule and NIH Policy on clinical trial disclosure in ClinicalTrials.gov. With focused and expert led videos, the course provides comprehensive training for new learners and on-demand access for more experienced members of your organization. The course also serves as a useful side-by-side companion when entering data into the Protocol Registration and Results System (PRS).

It will consist of eight modules cover understanding the regulations, how to navigate the data entry interface, protocol registration, and submitting summary results information.

Sign up to receive more information upon the course's release.