Protocols are submitted via the Cayuse Human Ethics (HE) module, an online protocol management software system, accessible through the College’s Okta Single Sign-On (SSO) portal. PIs should build time ...

Occasionally, researchers will need to submit their research to more than one research committee. This guidance addresses when submitting to the IBC and IRB is required. IRB and IBC review can be ...

The Purdue University Human Subject Protection Program is undergoing an internal assessment to ensure compliance with the institution's Federalwide Assurance. Researchers who have studies where IRB ...

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 mission of Pratt Institute’s Human Research Subjects Committee / Institutional Review Board (IRB) is to ensure quality research involving human subjects conducted under the auspices of the ...

Presented by Mississippi State Office of Research Compliance and Security staff, this training is appropriate for all faculty, staff and students involved in research activities. If you are a student, ...

The IRB Module provides a streamlined way for researchers to create and submit protocols for studies involving human subjects. It provides support for initial submissions, modifications, reportable ...

Winter Park, Florida--(Newsfile Corp. - November 24, 2025) - ADIA Nutrition, Inc. (OTCQB: ADIA) announced today that, following the independent Institutional Review Board's (IRB) acceptance of its ...

As of Sept. 12, 2023, Case Western Reserve University and the Cleveland Clinic Foundation have entered into a Mutual Non-Disclosure Agreement (Protocol Sharing with Marking Requirement). This ...

As the curtain closed on 2024, FDA issued a new draft guidance to assist clinical trial sponsors, investigators, and institutional review boards (“IRBs”) with defining, identifying, and reporting ...