Clinical Trials.gov Training: Protocol Registration & Results Reporting System (PRS)
The CTSI is pleased to announce a training opportunity for faculty and staff on ClinicalTrials.gov’s “Protocol Registration and Results Reporting System (PRS)”. The program examines the registration process and gives participants hands-on experience with results reporting. Whether you are new to the system, would like a refresher, or just need some helpful tips, this 2 ½ hour course covers everything you need.
Objectives
Demonstration of the PRS protocol registration process
Identify common errors and issues leading to ClinicalTrials.gov reviewers requesting modifications
Entering Results into PRS using a mock study
Data collection requirements for successful results reporting
Registration is required for this training. You will receive an account in the PRS Test environment.
NIH Funding Acknowledgment:Important Reminder – Please acknowledge the NIH when publishing papers, patents, projects, and presentations resulting from the use of CTSI resources by including the NIH Funding Acknowledgement.
