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 ...

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 ...

If you are submitting a grant to the National Institutes of Health (NIH) or the National Science Foundation (NSF), you may receive a notification that your study is likely to be funded and that more ...

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 ...

The approval represents a critical step in the clinical trials process, on Else’s pathway to launching a new infant formula in the US based on Else’s patented plant-based formula VANCOUVER, British ...

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 ...

What is IRB approval and why is it needed for my research project? Research involving human study includes the collection of data about or from human subjects and the use of existing data or specimens ...

All human research studies conducted by personnel affiliated with the University at Buffalo must be submitted to the Institutional Review Board (IRB) for review and approval. Research cannot commence ...

AUSTIN, Texas--(BUSINESS WIRE)--As the field of cognitive care expands, the aging global population is bringing heightened attention to neurodegenerative diseases like Alzheimer's and other forms of ...

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 ...

Research studies may result in the implementation of unapproved changes to IRB-approved research plans or failure to comply with established regulations, policies, and procedures. Any action or ...