Policies

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

This is a policy and procedure document describing the general qualifications, roles, and responsibilities of a Principal Investigator conducting a research project with human

This is a policy and procedure document outlining the exemption category of review for research involving human participants.

This policy and procedure document defines and lays out the proper procedures for reporting and reviewing noncompliance related to IRB protocols.

Note: this SOP has not been updated since 2010, and the logistics for submitting a closure request have since changed. See these instructions for how to submit a request to close a

Guidance from the Cornell IRB on developing an oral consent script, for those studies where a written and signed informed consent form is not appropriate.