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ClinicalTrials.gov PRS Training

ClinicalTrials.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). This program will walk participants through the registration process and results reporting while highlighting key components, requirements, and deadlines. Participants will learn about the current policies and laws related to registration and results reporting, as well as common errors and issues addressed by the PRS Quality Review team.


  1. Develop an understanding of the laws and polices related to registration and results submission on ClinicalTrials.gov PRS: What, why, which studies, and when
  2. Overview of the PRS protocol registration process, record maintenance, and results submission
  3. Identify common errors and issues encountered during the PRS Quality Review
  4. Understand MCW compliance requirements


Due to room size limit, we will give preference for in-person attendance to the first 25 registrants who select that option; others will be provided with virtual attendance information.

Attended Audience

Any staff, faculty member, resident, or fellow responsible for the registration and maintenance of ClinicalTrials.gov records.

Upcoming Sessions

A completion certificate is available upon request for participants who attend at least 80% of the course. Participants may use contact hours for maintaining ACRP and SOCRA certification.

Questions: Please contact Sarah Beyler (sbeyler@mcw.edu).

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.


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