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Guidance provided by the Cornell IRB on changes to compliance with human subjects research under the...
This is a guidance document to help researchers understand the IRB review process and what research ...
This is a guidance document to help reviewers understand the exemption category of review for resear...
This is a guidance document to prepare an application involving physiological devices, biomedical pr...
This is a guidance document to help researchers prepare applications to the IRB that involve the use...
This is the charge of the Institutional Review Board (IRB) for research involving human participants...
This is a guidance document for initial and continuing review by the IRB including requirements for ...
This SOP sets forth the definitions and examples of unanticipated problems (UPs) and adverse events ...
This policy sets forth the definition and examples of noncompliance; the procedures for reporting an...