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Clinical Trials.gov PRS Training

Protocol Registration and Results Reporting

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.

PARTNERS

VersitiChildren's Hospital of WisconsinVA Medical CenterMarquette UniversityMSOEUWM