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, ...

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 ...

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 ...

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 ...

The UAB Institutional Review Board for Human Use (IRB) is a committee established under federal regulations for the protection of human subjects in research (45 CFR 46). Its purpose is to help protect ...

Federal regulations mandate that information given to potential research participants or their representatives be in a language that they can understand. Translation of research documents, thus, is ...

RALEIGH, N.C.--(BUSINESS WIRE)--Univo IRB, a leader in ethical review and oversight for clinical research, is proud to announce the launch of its Canadian research ethics board (REB) review services.

The University IRB uses consultants to supplement IRB review when a specific project requires expertise beyond the scope of IRB membership. For example, a project/package may require: scientific or ...

The Institutional Review Board is a local review board, established by the Western Michigan University Board of Trustees in accord with federal regulations, to interpret and apply federal regulations, ...

The Food and Drug Administration announced on Tuesday that it would not regulate “IRB shopping,” a practice in which sponsors of clinical trials choose to submit proposed research to institutional ...