IRB Guidance Information
Documents
- Waiver of Informed Consent when Using Medical Records or Other Secondary Data or Specimens
- Unanticipated Problems and Adverse Events
- 10 Things Directors of Undergraduate Studies at UNC-CH Should Know about the IRB
- Navigating the IRB Process for Faculty Advisors
- Navigating the IRB Process for Students
- IRB Essentials Fact Sheet
Video Presentations
Network for Research Professionals: Orientation Series for New Coordinators
- Module 1 – Intro, Education, IRB
- Module 2 – Study Start Up, Personnel, GCP, Informed Consent
- Module 3 – Contracting, CT.gov, BCA, Budgeting, Essential Documents
- Module 4 – COI, Grant Budget Development, Investigational Drug and Device Policies, Additional training – HIPAA & Epic
- Module 5 – Recruitment, Putting it all together: from CDA to study close out
- Module 6 – UNC Orientation for New Clinical Research Personnel
Office for Human Research Protections (OHRP) Educational Videos
- The Research Clinic
- Research Use of Human Biological Specimens and Other Private Information
- General Informed Consent Requirements
- Institutional Review Board (IRB) Membership
- Complex Issues with Research Involving Vulnerable Populations
- IRB Records
- IRB Records II
- Preparing for an OHRP Compliance Evaluation
- When the Assurance Comes A Knockin’: OHRP’s FWA and IRB Registration Processes
Ethical Standards
- Belmont Report Educational Video
- The Belmont Report (Part One: Basic Ethical Principles)
- Nuremberg Trials History Channel documentary