IRB Updates

IRB Tips

IRB Reviewer Tips

IRB Tools

IRB Research Links

IRB UPDATES

• IRB SOP 1.4 (Studies Requiring Review) (3/5/2008)

• IRB SOP 2.6 (Reporting to Appropriate Federal Oversight Bodies, Institutional
  Officials and Research Sponsors) (3/5/2008)

• IRB SOP 7.5 (Expedited Review) (7/28/2008)

• IRB SOP 7.6 (Continuing Review) (7/28/2008)

• IRB SOP 8.1(Changing Study Protocol/Modifications to Previously Approved
  Research) (3/5/2008)

• IRB SOP 9.1 (Range of IRB Decisions) (7/28/2008)

• IRB SOP 10.2 (Unanticipated Problems Involving Risks to Participants or Others -- Investigator Reporting Requirements and IRB Actions) (7/28/2008)

• IRB SOP 12.5 (Reports of Potential Non-compliance) (3/5/2008)

• IRB SOP 12.6 (Findings of Non-compliance Under IRB Policy 12.5) (3/5/2008)

• IRB SOP 15.1 (Elements of Informed Consent Documents and Process) (7/28/2008)

• IRB SOP 15.3 (Waivers of Signed Informed Consent Documents and Waivers of Informed Consent Elements (3/13/2008)

• IRB SOP 15.4 (Non-English-Speaking Research Subjects) (7/28/2008)

• SOP 17.1 (Children in Research) (6/13/2008)

• IRB SOP 17.8 (Pregnant Women, Fetus, and Human In Vitro Fertilization) (3/13/2008)

• IRB Standard Operating Procedures -- Full Version
  
   

IRB TIPS

• New Standard Operating Policy 20.1: Questions, Concerns, Suggestions and
  Complaints (8/21/2007)

• Informed Consent Document and Process Policy Updates (7/30/2007)

• How to Add Staff to a Protocol in ARIA (6/13/2007)

• Exempt Continuing Review Reports Now in ARIA (6/5/2007)

• Curriculum Vitae in ARIA (12/5/2006)

• Submitting Case Reports to the UAMS Institutional Review Board (11/2/2006)

• IRB Tips Archive

IRB REVIEWER TIPS

• Continuing Review Intervals -- When Might It Need To Be More Often Than
  Annually? (6/1/2005)

• IRB Reviewer Tips Archive

IRB TOOLS

• Abbreviations and Acronyms

• HIPAA Authorization (MS Word)

• How to Sign Conflict of Interest Documents Electronically

• How to Submit a Research Protocol

• IRB Checklists for Review

• IRB Forms and Reference Materials

• IRB Review Fees

• PRISM Readability Toolkit for Research Investigators (Group Health Center for Health Studies, University of Washington)

• Short Written Consent/Assent for Non-English Speaking Minor or Minor's Parent: English Version (MS Word)

• Short Written Consent/Assent for Non-English Speaking Minor or Minor's Parent: Spanish Version (MS Word)

• Short Written Consent for Non-English Speaking Adult: English Version (MS Word)

• Short Written Consent for Non English Speaking Adult: Spanish Version (MS Word)

IRB RESEARCH LINKS

• Arkansas Children's Hospital Research Institute

• National Bioethics Advisory Commission

• OHRP Informed Consent Checklist

• OHRP Informed Consent Tips

• UAMS Policy on Conflict of Commitment and Conflict of Interest

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