WIRB | Western Institutional Review Board

Regulations Affecting Clinical Research, Including HIPAA

Requirements for Human Subject Protection Training

Conflicts of Interest

Site Staff Levels

Informed Consent

Adverse Events, Protocol Variances, and Unanticipated Problems

Continuing Review Activities and Reports

Guide for Researchers

IRB Jurisdiction

Guidelines for Writing a Research Protocol

Special considerations for Drug Research

Special considerations for Device Research

Special considerations for Behavioral Research

Special considerations for Multi-Center Studies

WIRB Review of Research Outside the U.S. and Canada

IRB Review

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Exemption Determinations

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History of WIRB

Statement of Compliance

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WIRB International Fellows Program

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WIRB Workflow Diagram

Screening Materials

Generic Materials

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Screening Materials
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