Researcher Resources
- OHRE Overview of Research Subjects’ Protections at UNC-CH (TBA)
- UNC Responsibilities of Staff in Human Subjects Research
- UNC IRB Process
(Other Links at UNC-CH Related to Human Subjects Research—drop title, left in as a guide of where to find on webpage)
-
- IRB Review Fee for Industry-Sponsored Studies
- NRP New Coordinator Orientation (recordings of 5 workshops sponsored by NC TraCS, UNC OCT, and NCRP)
- Environment, Health and Safety
- Radiation Safety and the Radiation Safety Committee
- Biological Safety and the Institutional Biosafety Committee
- Oncology Protocol Review Committee
- Investigational Drug Service (IDS) Note: This web site is on an intranet, and access may not be possible from some locations.
- UNC Hospitals Policy on Investigational Devices
- Office of Clinical Trials
- Registering an Investigator-Initiated Clinical Trial in a Public Registry
- UNC-CH NC TraCS Institute DSMB
- Information for Researchers from Research at Carolina
- Registering an Investigator-Initiated Clinical Trial in a Public Registry
- Relying on Central IRBs
- HIPAA Resources for Researchers
- Data Use Agreement Guidance
- Certificate of Confidentiality
- Unanticipated problems & Adverse Events
- Office for Undergraduate Research (OUR)
- Federal Regulations