Welcome to The Office of Research Regulatory Affairs!

The Office of Research Regulatory Affairs (ORRA) is a diverse team of experienced professionals who serve the UAMS research community.  We provide assistance with:

  • Regulatory submissions to the FDA (IND, IDE)
  • Quality assurance (GLP, GMP, GTP)
  • Clinical trial monitoring
  • Clinical trial registration

Please contact us if you believe we can be of assistance to you.

In The News…

  • Publication and reporting of clinical trial results:  cross sectional analysis across academic medical centers.
  • Failure to Report:  A STAT Investigation on
  • CT.Gov Offers New Individualized Training to Investigators for Results Module
  • FDA issues guidance on Risk Based Monitoring
  • Free GCPartner App now available for researchers
  • 23 Million Hours Spent Each Year Complying with Clinical Trial Requirements, FDA Estimates

For more news to know, go to ORRA news.

 Upcoming Training Opportunities…

SOCRA Workshop: Changes to, Tuesday, February 28, 2017, 11:00 AM-12:00 PM

See the ORRA Calendar for details on all training opportunities coming soon.