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
• Assigning Reviewers and the use of Consultants
• Conduct and Expectations of the IRB Members
• Conflict of Interest - IRB Committee Members
• Continuing Review of Previously Approved Projects (CPRs)
• Conversion Continuing Progress Reports (CPR)
• Emergency use of Investigational Drugs, Devices or Biologics
• Informed Consent for Human Subject Research
• Initial Review and Primary Reviewer Responsibilities
• Institutional Review Board Actions
• Institutional Review Board Committees
• Institutional Review Board Records
• International Studies
• Legally Authorized Representatives (LAR's) Who Can Consent on Behalf of an Adult Subject with Decreased Decisional Ability
• Meeting Minutes
• Multi-Center Projects and Coordinating Centers
• Planned Emergency Research
• Privacy and Confidentiality
• Projects Deferred to National Cancer Institute Central IRB (NCI CIRB)
• Public Data Sets
• Reconcile Federal Grants & Contracts policy
• Recruitment and Enrollment of non-English or Limited English-Proficient Subjects
• Research involving Pregnant Women and Children
• Research involving Prisoners
• Research with Subjects Likely to Manifest or Develop Decreased Decisional Ability
• Review and evaluation of IRB member service
• Review and evaluation of National Cancer Institute Cooperative Group Consent Forms 
  •  Modifications to the NCI Cooperative Group Informed Consent
• Review of Modifications to an Approved Project (Amendments)
• Review of Not Human Subject, Exempt, and Expedited Projects
• Review of Reportable Events
• Review of Treatment Use Requests
• Use and Requests to Quality Assurance Quality Improvement

MCW/FH IRB Committee Member Guidelines

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