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, ...

The University IRB follows federal regulations and guidance for reporting unanticipated problems involving risks to participants or others (Unanticipated Problems), serious or continuing noncompliance ...

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 ...

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 ...

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 ...

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 ...

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 ...

Who needs to submit an application to the IRB? All faculty, staff, and students conducting research with human subjects that does not meet the criteria for Classroom Research must submit an ...

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 UAB Human Research Protection Program (HRPP) is a committee established under federal regulations for the protection of human subjects in research (45 CFR 46). Its purpose is to help protect the ...

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 ...