IRB Member Responsibilities

• Brief Responsibilities of an HS-IRB Member
• Brief Responsibilities of an MR-IRB Member

Forms

• HS-IRB and MR-IRB Reviewer Form
  
• Initial Review Pre-Review Checklist
  
• Continuing Review Checklist for Staff and Primary Reviewers
• Checklist for Review of VA Protocols
• Sponsor Notice of VA Protocol Expiration of IRB Approval
  
  

IRB Member Fact Sheets

• Belmont Report
• Brief Overview of Regulatory Basis of IRB Authority & Review Responsibilities
• Continuing Review & Changes of Protocol
• Criteria for IRB Approval
• Informed Consent Process, Elements, and Waivers
• Investigator Conflicts of Interest
• IRB Member Conflicts of Interest
• IRB Responsibilities Related to Review of VA Research
• Noncompliance & Protocol Exceptions and Deviations
• Overview of the Accreditation Process and UW-Madison’s Human Research Protections Program
• Privacy and Confidentiality
• Regulations for Research Involving Children
• Regulations for Research Involving Pregnant Women, Fetuses, and Neonates
• Regulations for Research Involving Prisoners
• Regulations for Unapproved Drugs, Biologies, and Devices
• Review Processes Other than Full Board
• Unanticipated Problems & Serious Adverse Events

IRB WebKit Helper Application

• Internet Explorer (6.0 and 7.0)
• Mozilla Firefox
• Safari

Click here to log on to IRB WebKit Helper Application

Meeting Dates and Deadlines

• HS-IRB and MR-IRB Meeting Dates and Submission Deadlines

UW-Madison Human Research Protection Program

• Human Research Protection Program Guidance
• Human Research Protection Program Policies