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
  • Contract review, negotiation and approval
  • Clinical trial registration

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

Campus 3

In The News…

  • 23 Million Hours Spent Each Year Complying with Clinical Trial Requirements, FDA Estimates
  • NIH extends public comment period for the NPRM on Clinical Trials Registration and Results Submission!!
  • FDA issues guidance on Laboratory Developed Tests.

For more news to know, go to ORRA news.

 Upcoming Training Opportunities…

  • March  19, 2015:  11:00 am to Noon, COPH G226, Title “Expanded Access” presented by Melisa Clark

See the ORRA Calendar for training opportunities coming soon.