Human Research Protection Program

MCW/FH IRB Committee Member Procedures and Guidelines

Committee Member Procedures | Committee Member Guidelines

MCW/FH IRB Committee Member Procedures

• Advertisements, Recruitments Methods and Compensation (pdf)

• Assigning Reviewers and the use of Consultants (pdf)

• Conduct and Expectations of the IRB Members (pdf)

• Conflict of Interest - IRB Committee Members (pdf)

• Continuing Review of Previously Approved Projects (Continuing Progress Reports) (pdf)

• Emergency use of Investigational Drugs, Devices or Biologics (pdf)

• Informed Consent for Human Subject Research (pdf)

• Initial Review and Primary Reviewer Responsibilities (pdf)

• Institutional Review Board Actions (pdf)

• Institutional Review Board Committees (pdf)

• Institutional Review Board Records (pdf)

• Legally Authorized Representatives (LAR's) Who Can Consent on Behalf of an Adult Subject with Decreased Decisional Ability(pdf)

• Meeting Minutes (pdf)

• Planned Emergency Research (pdf)

• Privacy and Confidentiality (pdf)

• Reconcile Federal Grants & Contracts policy (pdf)
   
• Recruitment and Enrollment of non-English or Limited English-Proficient Subjects (pdf)

• Research involving Pregnant Women and Children (pdf)

• Research involving Prisoners (pdf)

• Research with Subjects Likely to Manifest or Develop Decreased Decisional Ability (pdf)

• Review and evaluation of IRB member service (pdf)

• Review and evaluation of National Cancer Institute Cooperative Group Consent Forms (pdf)
  o Modifications to the NCI Cooperative Group Informed Consent (doc)

• Review of Modifications to an Approved Project (Amendments) (pdf)

• Review of Not Human Subject, Exempt, and Expedited Projects (pdf)

• Review of Reportable Events (pdf)

• Review of Treatment Use Requests (pdf)

• Use and Requests to Quality Assurance Quality Improvement (pdf)

MCW/FH IRB Committee Member Guidelines

•  Guidelines for Determining "Exempt" and "Expedited" Eligibility (pdf)