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 ...
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 ...
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 ...
To comply with the 21st Century Cures Act, 1 the Food and Drug Administration (FDA) has released two Notices of Proposed Rulemaking (NPRMs). NPRMs are the initial public notice of a proposed change to ...
Rollout of the Purdue Excellence in Research Administration (PERA), Purdue’s innovative electronic research administration system, continues with the upcoming launch of the Institutional Review Board ...
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 ...
Research that meets an exemption should be submitted via the online form corresponding to the appropriate exemption (see this link to determine which of the exemptions applies to your research, if any ...
Below is a list of guidance/policies developed by the W&M IRB. To find specific guidance, you can use the "control F" (Dell computers) or "command F" (Mac computers) feature on your computer to search ...
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 ...
RALEIGH, N.C.--(BUSINESS WIRE)--Univo IRB, a leader in ethical review and oversight for clinical research, is proud to announce the launch of its Canadian research ethics board (REB) review services.
Prior IRB approval must be obtained for all amendments or modifications to research previously approved by the full committee or via expedited procedures unless immediate changes are necessary to ...
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