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IRB Procedure Library

Procedure 7: Renewals, Amendments, Closures, and Transfers

The purpose of this procedure is to detail W&M’s procedure to address W&M’s IRB’s standard for the continuing review, renewal, closure, or transfer of an IRB-approved research protocol.

Procedure 9: Local and Participant Context Review

The purpose of this procedure is to detail William & Mary’s procedure to address the review of research that involves people considered contextually vulnerable or those in international settings This document details information regarding the additional review procedures, how they occur, and what they contribute to the IRB review process.

Procedure 3: Expedited Review of Human Subjects Research

The purpose of this procedure is to detail William & Mary’s procedure to address the IRB’s standard and operating practices for the conduct of expedited reviews. This document outlines the processes of preparing, conducting, and documenting expedited reviews.

Procedure 4: Review and Approval for Clinical Trials

The purpose of this procedure is to outline W&M’s process for addressing research involving human subjects that also meets the criteria for a clinical trial. Clinical trials must comply with requirements that do not apply to other types of human subjects research. These requirements are designed to address the increased participant vulnerability and risks associated with many clinical trials compared with other research.

Procedure 8: Review and Approval for Cooperative Research

The purpose of this procedure is to detail W&M’s procedure to address multi-site or cooperative research with human subjects completed by W&M researchers. In this document, you will find the policy and standard operating procedures for the use of reliance agreements and how the W&M IRB facilitates cooperative research.