Case Report Form (CRF)/Source Document templates were created for University of Wisconsin-Madison researchers. The forms serve only as templates, and must be edited to meet the study data collection needs as described in the protocol.
- Demographics
- Eligibility Checklist
- Medical History (General) Form Template
- Informed Consent/HIPAA Authorization Documentation
- Concomitant Medication Tracking Log
- Physical Examination
- Vital Sign Measurements
- Electocardiogram Results
- Inclusion Exclusion Checklist Form Template
- Device Accountability Log (per protocol)
- Drug Accountability Log (per protocol)
- Drug Accountability Log (per subject)
- Research Sample Tracking Log Template
- Adverse Event Tracking Log
- Serious Adverse Event (SAE) Log (Per Subject)
- Serious Adverse Event (SAE) Log (per protocol)
- Combined AE-SAE Tracking Log Template
- Protocol Deviation/Unanticipated Problem Log
- Telephone Contact Documentation
- Subject Off Study Form
- Note to File Template