Resources Related to UNC Research
The links below provide useful resources on IRB and related issues.
Other Links at UNC-CH Related to Human Subjects Research
- Carolinas Collaborative Research Guidance Document
- Required Costs – UNC Research
- Clinical Translational Research Center (CTRC) Orientation and Training
- Environment, Health and Safety
- Oncology Protocol Review Committee
- Office of Clinical Trials
- Registering an Investigator-Initiated Clinical Trial in a Public Registry
- Conflict of Interest:
- UNC-CH NC TraCS Institute DSMB
- Information for Researchers from Research at Carolina
- HIPAA Research Policy
Federal Office for Human Research Protections
- Office for Human Research Protections. Federal agency that regulates IRBs and human subjects research.
- The Code of Federal Regulations (45CFR46). Federal regulations governing protection of human subjects
- OHRP Guidance on Unanticipated Problems and Adverse Events
- OHRP’s Frequently Asked Questions
- Expedited Review Categories of Research
- IRB Guidebook
- OHRP Policy Guidance by Topic
- OHRP Guidance on Coded Private Information and Biological Specimens
- NIH Decision Chart on Applying OHRP Guidance on Coded Info/Specimens
- Engagement of Institutions in Research
- Links to reference documents, historical materials and Common Rule departments/agencies. A list maintained by OHRP.
Other Federal Agencies
- Centers for Disease Control and Prevention
- Department of Education
- Department of Health and Human Services
- Office for Civil Rights – HIPAA
- Office of Research Integrity
- Office of Minority Health announces the release of a new resource to aid researchers: The Compendium of Publicly Available Datasets and Other Data-Related Resources (Compendium). This is a free resource that compiles in one place descriptions of and links to 132 public datasets.
- Food and Drug Administration
- 21CFR50. FDA regulations for protection of human subjects
- 21CFR56. FDA regulations governing IRBs
- FDA Information Sheets: Guidance for IRBs, and Clinical Investigators and Sponsors
- FDA Guidance on Adverse Event Reporting to IRBs
- FDA Guidance on IND Safety Reports
- Investigational Device Exemption (IDE)
- Drug Approval Application Process
- Expedited Review List
- Frequently Requested ORA Documents under FOIA
- Index of Categories of Documents for Electronic Reading Room
- Information for Clinical Investigators
- Regulatory Guidance
- FAQs about Medical Devices
- In Vitro Diagnostic Studies Using Leftover Specimens
- National Institutes of Health
- Ethical Issues in Research Involving Human Participants
- Office of Biotechnology Activities
- National Cancer Institute
- National Human Genome Research Institute
- National Institutes of Environmental Health Sciences
- National Library of Medicine
Non-Governmental Organizations
- American Council on Science and Health
- Public Responsibility in Medicine and Research (PRIM&R)
- Association for the Accreditation of Human Research Protection Programs (AAHRPP)
- “Reaching Beyond Regulations: The Pursuit of Accreditation for Human Research Protection Programs.” Lynn E. Smith, JC. CIM, CIP. Monitor, June 2008, 67-70.
- Association of American Medical Colleges
- Association of American Universities
- Children’s Hospital Boston’s Interactive Parents’ Guide to Medical Research
- Family Health International. See their Research Ethics Training Curriculum
- Harvard Program on Ethical Issues in International Health Research
- The Hastings Center
- Kennedy Institute of Ethics
- National Academy of Sciences
- Institute of Medicine
- National Research Council