About ORO |
ORO Correspondence |
ORO Checklists |
Research Compliance Officer Education |
ORO Policy Documents |
Get Connected |
Human Subjects Protections & FWAs |
Animal Welfare |
Research Misconduct |
Research Safety |
Teleconference Minutes |
ORO Home
| VA Home
| About VA
| Organizations
| Apply Online
| Find a Facility
| Contact VA
| Health Care
| Benefits
| Burial & Memorials
| Graphical Version
ORO
IRB SOPs
Search Educational Opportunities Glossary of Terms Staff Directory
| [ IMAGE : (local) tn_balls3.gif ] | Human Research Protection Program Best Practices Guide: Human Subjects Institutional Review Board Standard Operating Procedures (developed by ORCA in consultation with PricewaterhouseCoopers LLP in September 2001) |
| [ IMAGE : (local) tn_balls3.gif ] | The Office for Human Research Protections (OHRP) has posted guidance regarding written Institutional Review Board (IRB) procedures. In order to assist institutions in developing adequate written IRB procedures, OHRP has compiled a summary of the relevant regulatory requirements and guidance issued routinely by OHRP over the past several years. This new OHRP guidance, dated July 11, 2002, can be found athttp://www.hhs.gov/ohrp/humansubjects/guidance/irb71102.pdf. |
Español | VA Forms | Locations | Contact the VA | Frequently Asked Questions (FAQs)
Privacy Policy | Web Policies & Important Links | Freedom of Information Act
Annual Performance and Accountability Report | Small Business Contacts | Site Map
USA.gov | White House | USA Freedom Corps
Reviewed/Updated Date: May 11, 2005