Single IRB Review is an arrangement in which one institution's IRB provides review, approval and oversight for the Human Research activities of multiple institutions. This is intended to streamline ...

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

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 Institutional Review Board (IRB) will now utilize the online submission platform, Research Enterprise Solutions (RES), for NEW human subjects research applications. New IRB studies will no longer ...

Univo IRB today announced a partnership with The Patient View to provide essential patient insights that will improve clinical trial participation and retention for sponsors and CROs. By engaging with ...

The University IRB adheres to the regulatory requirements for research which involves a prisoner as outlined in 45 CFR 46 Subpart C. Federal regulations consider prisoners to be a vulnerable ...

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 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 ...

New Release of Advarra's Study Collaboration Solution Provides Sponsors and CROs a Single View into the Progress of Site Activation Milestones and IRB Review Status Across Sites COLUMBIA, Md., April ...

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 ...