Regulatory Knowledge - Alternative IRB Model Pilots
Description: |
The mission of the Alternative IRB group is to improve the efficiency of implementing clinical trials. To accomplish this goal, the group will explore pilot studies of alternative IRBs within the CTSA Consortium, gather and share information on local cooperative agreements within the Consortium, study and improve the process of protocol and informed consent document approval within the Consortium, and gather and share data on the metrics of protocol approval, implementation, and enrollment. |
Alternative IRB Model Pilots Participants:
| NIH Coordinator(s) |
Daniel Rosenblum (NCRR) Jody G. Sachs (NCRR) |
| Participation | Click to view |
| Previous Meetings (2007) |
August 15, 2007
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