Registering your study with ClinicalTrials.gov and entering study results are necessary steps for investigators to be compliant with regulations. This UB CTSI Educational Modules video takes a close look at the Protocol Registration and Results System (PRS) and explores:
Developed by Lynn Jagodzinski, CTSI Clinical Research Regulatory Administrator, and Urmo “Mo” Jaanimägi, CTSI Quality Assurance Specialist, UB Clinical and Translational Science Institute
Presenter: Urmo “Mo” Jaanimägi, CTSI Quality Assurance Specialist, UB Clinical and Translational Science Institute
Running Time: 15 minutes
Posting Date: March 29, 2022
Questions?
Contact Lynn Jagodzinski, UB CTSI Clinical Research Regulatory Administrator, at lynnjago@buffalo.edu, or UB CTSI Quality Assurance Specialist Urmo “Mo” Jaanimägi at uj@buffalo.edu.
Additional resources:
University at Buffalo’s ClinicalTrials.gov Registration and Results Guide: download
PRS Guided Tutorials:
How to Report:
Basic Results Data Elements Definitions:
PRS User Guide: Located on Main Menu (Help) in database
All Training Materials:
10 Minute Webinars for each results module:
Checklists and Templates (for each scientific module):
Helpful Hints (with common study designs examples):
Glossary: