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IRB/Grant Submission

Consultation providing a regulatory and ethics perspective through the IRB process

The Institutional Review Board (IRB) review process is often times perceived as the primary rate-limiting step to conducting clinical and translational research. Regulatory Knowledge and Support (RKS) consultation may be able to shorten the time to approval with its experience and particular regulatory and ethics perspective.

Clinical research coordinators and investigators can request a consult for BUCK-IRB submission training and associated concerns.

This service is complementary to the assistance provided by the University’s Office of Responsible Research Practices (ORRP) and to the University’s overall Human Research Protection Program.

Request a Service

Related Services Related Pages Related Programs

Protocol Consultation
Data and Safety Monitoring
Research Subject Advocate
Consent Document Preparation
MultiCenter IRB Review
Research Ethics
Accelerated Research Agreements Initiative

IND/IDE Support
Good Clinical Practice Training
Acknowledging CTSA grant support in publications

Regulatory Knowledge & Support

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