Forms & Templates
The CRCO is actively creating and connecting to forms and templates that promote regulatory compliance and best practices in clinical research. Explore these resources by topic.
- Feasibility Assessment
- Standard Operation Procedure/Work Instruction Templates
- Data Managment
- Informed Consent Process
- Investigational Product (IP) Accountability Standard Operating Procedure and Work Instructions
- Management and Reporting Adverse Events
- Training
- FDA Part 11 Epic Certification
- Study Start-Up Checklist
- Guidance for Completing a Supervisory Plan for Clinical Research
- PI Supervisory Plan for Clinical Research
- Delegation of Responsibility Log
- Training Log
- Monitoring Plans
- Eligibility Checklist Template
- Participant Enrollment Documentation
- Informed Consent Process and HIPAA Authorization Documentation
- Enrollment Log
- Master Subject ID Log