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

IBC Services

Data and Safety Monitoring

Consultations

Exemption Determinations

Training

History of WIRB

Statement of Compliance

WIRB International Fellows Program

WIRB News

Career Opportunities

IRB Services

Fees

Board Actions

WIRB Workflow Diagram

Screening Materials

Generic Materials

Subject Recruitment Materials

Federally Funded Research

Continuing Review Report Forms (CRRFs)

Study Closure

Site Visits

Welcome to the WIRBNet Authenticated Web Portal.

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You may now submit 10-day Adverse Event Reports using a 'smart' web form.

To access this feature, go to 'WIRBNet Tracking'. Select the protocol and study then click the 'Submit an Adverse Event' button.