Explore UAB

Clinical Research

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 

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







Note: The classic ClinicalTrials.gov site will retire on June 25th, with it being permanently replaced by the Beta site. Click here to read more about ClinicalTrials.gov modernization.

Try out the new PRS beta home page, part of the ongoing ClinicalTrials.gov modernization.

New PRS beta Home Page

Questions?  EmailThis email address is being protected from spambots. You need JavaScript enabled to view it.

 





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
Grant Numbers/Secondary IDs

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