Policies

70 results

Policy

IRB Policy: #2 Submission Requirements and Procedures for Exemption IRB Review

This is a guidance document to help reviewers understand the exemption category of review for resear...

Policy

IRB Policy: #20 Use of Social Networking Sites or Mobile Devices for Human Participant Research

This is a guidance document to help researchers prepare applications to the IRB that involve the use...

Policy

IRB Policy: #3 Initial and Continuing IRB Review

This is a guidance document for initial and continuing review by the IRB including requirements for ...

Policy

IRB Policy: #4 Reporting Unanticipated/Adverse Events

This SOP sets forth the definitions and examples of unanticipated problems (UPs) and adverse events ...

Policy

IRB Policy: #5 Managing Noncompliance

This policy sets forth the definition and examples of noncompliance; the procedures for reporting an...

Policy

IRB Policy: #6 Suspension and Termination of research involving human subjects

This policy sets forth which persons/entities have the authority to enact a suspension or terminatio...

Policy

IRB Policy: #7 Reporting Unanticipated Problems, Noncompliance, Suspensions, and Terminations to Regulatory Agencies and Sponsors

The Institutional Official has delegated this reporting authority to the Director of Office of Resea...

Policy

IRB Policy: #8 Closure of a Research Protocol

This SOP sets forth the requirements for and process by which a PI should close their IRB protocol. ...

Policy

IRB Policy: #9 Recruitment and Payment of Human Participants in Research

The recruitment of human participants for a research study is seen by the IRB as the initial stage o...

Policy

IRB Policy: Clinical Trials Guidance

Guidance provided by the Cornell IRB for identifying and managing compliance for clinical trials inv...

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