In order for your IRB to access CIRB review documents and to utilize the facilitated
review
mechanism, your institution must formally enroll in the Initiative. To join the
Initiative, institutions
must have their own functioning
IRB;
be actively enrolling patients in Cooperative Group adult Phase 3 clinical trials -or- Pilot, Phase 2 or Phase 3 pediatric clinical trials;
The enrollment materials can be sent electronically or can be downloaded from this webpage. The Request for 30-Day NCI CIRB Website Access Form is available on this webpage for those interested in joining, but would like to review CIRB approved studies prior to joining.
CIRB Operations Office staff are available to assist you with the enrollment process at ncicirbcontact@emmes.com or toll-free at 1-888-657-3711.
