Comprehensive Template for Clinical Research Participation
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Study Title: [Insert Study Title] Principal Investigator: [Name, Credentials] Institution: [Institution Name] Study ID: [Protocol Number]
Name: ________________________ Date of Birth: ________________ Medical Record Number: ________
I, the undersigned, confirm that:
□ Participant has capacity to consent independently □ Legal representative/proxy consent required
Primary Contact: Name: ________________________ Relationship: __________________ Phone: ________________________
Participant Signature: _______________ Date: _______________
Witness Signature: _________________ Date: _______________
Investigator Signature: _____________ Date: _______________
Name: ________________________ Relationship to Participant: ________ Signature: _____________________ Date: _______________
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