All human subjects research connected with members of the Smith College community (either as researchers or study participants) must be reviewed and approved by the IRB prior to the initiation of the ...

A student can conduct human subjects research under the supervision of an experienced faculty advisor. The faculty advisor must be identified on the student PIs initial submission as the principal ...

There is often confusion as to which classroom projects and independent student projects must be reviewed by the Institutional Review Board. Generally, a student project involving human subjects falls ...

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 ...

A single IRB (sIRB) of record will be used in the ethical review of non-exempt human subjects research protocols funded by federal agencies that are carried out at more than one site in the United ...

The full Case Western Reserve University Institutional Review Board (IRB) meets once per month. Meeting dates and deadlines can be found here. An investigator should expect a protocol requiring full ...

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 ...

CARY, N.C., Sept. 15, 2025 /PRNewswire/ -- WCG, a global leader in providing solutions that measurably improve and accelerate clinical research, today announced the launch of WCG ClinSphere™ eReview ...

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The US Food and Drug Administration (FDA) last week issued draft guidance offering insights to sponsors and institutional review boards (IRBs) on the process for referring research involving children ...