Central Oregon's Regulatory Body to
Assure Human Subject and Biomedical Research Protections

Purpose, Table of Contents, Meeting Schedule, Applications Submission Deadlines, Additional Information

Regulated, Guided and Audited by the Food and Drug Adminstration (FDA) and Department of Human and Health Services (DHHS) Office of Human Research Protections (OHRP) and by relevant Oregon Law

   Federal regulations, guidances and FAQ answers 
   Clinical trials monitored by the IRB since 2005 
   Current IRB members and staff

 *IRB meeting schedule & application deadlines
 *Continuing Renewal Application Due Dates
 *IRB policies and procedures 
 *Application forms and related documents
 *2010 Master Plan
 *Online Course in clinical trials and human research protections
**IRB meeting documents: agendas, meeting packets, minutes**

  *Access limited to authorized members
**Access limited to IRB members & staff

To learn more about the SCHS IRB, contact the IRB Coordinator/Secretary at (541) 706-2900 x7878