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…

  • 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…

  • October 21, 2015:  Research Protocol Development.
  • October 22, 2015:  Information Quality, Principles of IQ.
  • October 26, 2015:  Protocol Deviations
  • October 28, 2015:  Reportable New Information and the IRB

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