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
- Data Use Agreement Guidance
- Review Process FAQ
Video Presentations
Network for Research Professionals: Orientation Series for New Coordinators
- Week 1 Module – Intro, Education, IRB PDF / Recording
- Week 2 Module – Study Start Up, Personnel, GCP, Informed Consent PDF / Recording
- Week 3 Module – Contracting, CT.gov, BCA, Budgeting, Essential Documents PDF / Recording
- Week 4 Module – COI, Grant Budget Development, Investigational Drug and Device Policies, Additional training – HIPAA & Epic PDF / Recording
- Week 5 Module – Recruitment, Putting it all together: from CDA to study close out PDF / Recording
- Week 6 Module – PDF / Recording
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
- OHRP: Reviewing and Reporting Unanticipated Problems and Adverse Events
Ethical Standards
- Belmont Report Educational Video
- The Belmont Report (Part One: Basic Ethical Principles)
- The Nuremberg Code: A Turning Point in the History of Bioethics
- Nuremberg Trials History Channel documentary
Human Subject Abuses
- Eva Kor – Survivor of the Holocaust and Nazi Experiments on Twins
- Iconic People: Eva Kor speaks about Auschwitz, medical experiments, and forgiveness
- Eva Kor: “Surviving the Angel of Death: The True Story of a Mengele Twin in Auschwitz”
- Michael Kor: Holocaust Survivor