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We are pleased that you are interested in partnering with us to provide human
subject protections for study participants in NCI-sponsored, Cooperative Group
clinical trials. To start the enrollment process download the Enrollment
Checklist, Enrollment Form, Authorization Agreement and Division of CIRB and
Local Responsibilities. Follow the steps outlined in the Enrollment Checklist
for incorporating the CIRB into your Institution.
If you need further guidance or have any questions please feel free to contact
the NCI CIRB Helpdesk at 1-888-657-3711 or via email
ncicirbcontact@emmes.com
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