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 ...

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 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 ...

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 ...

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The US Food and Drug Administration (FDA) last week issued draft guidance offering insights to sponsors and institutional review boards (IRBs) on the process for referring research involving children ...

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 ...

Navigating the Human Research Protection Program (HRPP) submission process just got easier! The Human Research Protection Program (HRPP) has launched a new Guidebook and Self-Determination Tools to ...

Minutes of IRB meetings will be prepared in sufficient detail to demonstrate that IRB meetings were convened with a quorum of members and IRB deliberations reflecting appropriate regulatory and legal ...