Due to the involved nature of the IRB review process, submitting research projects for review can prove to be challenging. In order to simplify the process and support investigators, the IRB has ...

Before submitting your study for IRB review, the School of Health Professions (SHP) requires completion of the Protocol Oversight Review Form (PORF). This step ensures your project has been reviewed ...

The University IRB has the authority to suspend or terminate IRB approval of research that is not being conducted in accordance with IRB requirements or that may pose unexpected, serious harm to ...

Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

Contact Valerie Bailoni, UB IRB Helpline, at ub-irb@buffalo.edu, or Alexis O’Brien , UB CTSI Clinical Research Facilitator, at ctsihelp@buffalo.edu . Human Research ...

Annual Conference is in the books, and the Food and Drug Administration’s (FDA) messaging at the 2026 edition blended ...

The Federal Policy for the Protection of Human Subjects or the “Common Rule” outlines specific regulations for human subjects research. The Common Rule is heavily based on the "The Belmont Report," ...

Investigators and IRBs must ensure that research (i.e., clinical investigation) involving investigational drugs or biologics is conducted in accordance with applicable federal regulations. These ...