At a Glance:
Clinical Trials Initiative

Poster CTI 2019

Contact

Tamara L. Howard 
Clinical Research Regulatory Coordinator II
tlhoward@uabmc.edu

Dunia F. Ritchey, M.Ed.
Clinical Research Regulatory III, FDA Submission Specialist, DSMB Administrator, Clinicaltrials.gov Administrator
dfritchey@uabmc.edu 

Sidebar Grant V3
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ClinicalTrials.gov Protocol Registration and Results System (PRS)FDAAA Trials Tracker



Log In to PRS: https://register.clinicaltrials.gov/
Need an account, advice, or help? Contact This email address is being protected from spambots. You need JavaScript enabled to view it.. 


   Helpful Hints:
  • Logging In – Organization: UAB
  • New Record – Unique Protocol ID is the UAB IRB number (IRB-3000#####)
  • Responsible Party – Principal Investigator
    Resources:
 
ClinicalTrials.gov External Resources:
Submit Studies to ClinicalTrials.gov PRS
Why Should I Register and Submit Results?
FDAAA 801 and the Final Rule
How to Apply for a PRS Account
How to Register Your Study
How to Edit Your Study Record
How to Submit Your Results
Frequently Asked Questions
Support Materials		 Podcasts (Learn on the Go):
Quick Start Guide
Record Summary
Study Status Home Page
Brief Description Guide
Arms & Interventions
Outcome Measures