Templates
The CRCO is actively creating and connecting to templates that promote regulatory compliance and best practices in clinical research. Explore these resources by topic.
- FDA Part 11 Epic Certification
- Feasibility Assessment Checklist
- PI Supervisory Plan for Clinical Research
- Comprehensive Monitoring Plan
- Concise Monitoring Plan
- Eligibility Checklist
- Informed Consent Process/Discussion Checklist
- Enrollment Documentation
- Enrollment Log
- Master Participant ID Log
Visit the NCCIH Clinical Research Toolbox for an A to Z repository of forms, logs, and checklists to inform clinical study start-up and conduct.
Standard Operation Procedures (SOPs) 
Below, you’ll find a curated list of SOP templates to streamline your research processes and maintain adherence to Good Clinical Practice (GCP) and FDA regulations.