I'm looking for info on OHRP compliance if you're willing to share it.
We're wondering how other institutions  are monitoring compliance with the
OHRP regs in their subcontracts.  Specifically, how are you insuring that
subgrantees that are engaged in humans subject research have an active
assurance?  Second, how do you monitor that the key personnel have completed
the OHRP education requirements?

Although this applies only to NIH, my university is applying this standard
to all projects involved in human subjects research.  Are you doing
likewise?

Thanks very much,

Maryellen O'Brien
Grant/Contract Specialist
Office of Research and Sponsored Programs
Rutgers University

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