When is IRB Approval Required? If your project involves "research" and "human subjects" as defined by 45 CFR 46, you must submit an application to the Case Western Reserve University Institutional ...

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 ...

The Human Ethics module of ROAMWyo will streamline all aspects of human subjects research: protocol submission, review, and approval, as well as provide a dashboard where researchers can view the ...

The Smith College Institutional Review Board (IRB) upholds the principles of respect, beneficence and justice, with established guidelines to ensure that human research participants are treated with ...

Research with human participants in countries outside the United States must comply ethical standards. Additional considerations may be required depending on the country of research. Furthermore, ...

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, ...

Any research that involves human subjects, whether funded or not, that is undertaken by a WIU faculty, academic staff or student or supported by Western Illinois University, must be reviewed by the ...

As the curtain closed on 2024, FDA issued a new draft guidance to assist clinical trial sponsors, investigators, and institutional review boards (“IRBs”) with defining, identifying, and reporting ...

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

MELBOURNE, Australia and NEW YORK, Jan. 17, 2024 (GLOBE NEWSWIRE) -- Incannex Healthcare Inc. (Nasdaq: IXHL), (‘Incannex’ or the ‘Company’), a pharmaceutical company developing unique medicinal ...