Policies

This is a policy and procedure document providing guidance for researchers preparing for human participant research involving physiological devices, biomedical procedures, or

This is a policy and procedure document outlining when Cornell IRB submission, review, and approval are needed, and the associated high level processes.

This is a policy and procedure document to help researchers prepare applications to the IRB that involve the use of social networking sites or mobile devices.

This is a policy and procedure document for initial, amendment, and continuing review by the IRB including requirements for submission, approval criteria, and expedited and

This policy and procedure document outlines the procedures that must be taken to suspend or terminate an IRB protocol.

This policy and procedure document outlines the procedures for complying with federally mandated reporting requirements concerning unanticipated problems, noncompliance, and

This is a policy and procedure document outlining the review of recruitment methods and materials by the IRB. Due to U.S. export regulations, Cornell researchers cannot send money

This is a policy and procedure document outlining the requirements for an effective informed consent process.

This policy and procedure document defines and lays out the proper procedures for reporting and reviewing unanticipated problems and adverse events related to IRB protocols.

This document sets forth the additional requirements for obtaining IRB approval for research involving normal, healthy participants, as well as special considerations concerning