Resource Library
The CRSO is developing and linking to resources supporting best clinical research practices. Browse resources by topic.
Browse by Topic
黑料网-Chapel Hill:
Other Sources:
Recruitment and Retention
黑料网-Chapel Hill:
Other:
- Recruitment and Retention Plan Document for Coordinating Centers (RIC 鈥� Recruitment Innovation Center, Trial Innovation Network (med.unc.edu/crso))
- Recruitment and Retention Plan Document for Sites (RIC 鈥� Recruitment Innovation Center, Trial Innovation Network (med.unc.edu/crso))
- 听
Informed Consent
黑料网-Chapel Hill:
- Checklist for Documenting the Informed Consent Discussion Template (SOM CRSO (med.unc.edu)
- Contextual Note for Documenting the Informed Consent Discussion in the Study Record Template (SOM CRSO (med.unc.edu))
- Contextual Note for Documenting the Informed Consent Discussion in the EMR Template (SOM CRSO (med.unc.edu))
- Elements of the Informed Consent Form and HIPAA Authorization (SOM CRSO (med.unc.edu))
- Tips on the Remote Consent Process (SOM CRSO (med.unc.edu))
Other Sources:
Education and Training
黑料网-Chapel Hill:
Other Sources:
Study Procedures
IRB听
Data and Safety Monitoring
- Data and Safety Monitoring Guidance For PI-initiated Research (黑料网-Chapel Hill SOM CRSO (med.unc.edu))
- DMC vs IRB: What鈥檚 the Difference? (Advarra (med.unc.edu))
Quality Assurance (QA)/ Quality Improvement (QI)
- Quality Assurance and Quality Improvement (QA/QI) FAQs (黑料网- Chapel Hill NC TraCS Regulatory, OHRE (med.unc.edu))
- Quality Assurance (QA) and Quality Improvement (QI) Screening Checklist (黑料网 Chapel Hill NC SOM CRSO, TraCS Regulatory, OHRE (med.unc.edu))
Roles and Responsibilities
Regulatory Forms and Templates
If you have questions or would like guidance and tips on a topic not already listed here, please email us at crso@med.unc.edu.