Additional Resources
- IRB Policies and Application Forms: Any research involving human subjects proposed by faculty, staff, or students must be reviewed and approved by an IRB before research may begin, and before related grants may be funded.
- UNC Lineberger Clinical Trials Office (CTO): The UNC Lineberger Clinical Trials Office (CTO) is the clinical research management team and turns research concepts into operational clinical trials
- Radiation Safety at UNC-Chapel Hill: Find radiation safety forms and learn more about radiation safety services at UNC-Chapel Hill.
- Biological Safety at UNC-Chapel Hill: Find information in the Biological Safety Manual provided by UNC-Chapel Hill Environment, Health and Safety division.
- Investigational Drug Services
- UNC Lineberger Comprehensive Cancer Center Institutional Data and Safety Monitoring Plan (last updated 12/20/2022)
- NCI: Common Terminology Criteria for Adverse Events v3.0 (CTCAE): Accurate and specific reporting of adverse events (AE) in clinical trials is critical to protecting patients and accurately determining the effects of new cancer treatments. Federal regulation requires all physicians who sign the FDA1572 Investigator Registration Form to document and report AEs. This is mandated by their clinical trial protocols, including the nature and severity (grade) of the event.