Study Management Resources and Tools
Amendments
Amendments to an approved protocol can be submitted at anytime.
Template Resources
Prospective Design Research Protocol Template
Retrospective Design Research Protocol Template
Not sure which basic design to select? Click here for a descriptive overview.
Other Resources
GCP – Essential Doc – Conduct Clinical Trial
Continued Informed Consent
Info Sheet – Clinical Coordinators
IRB Submission Tracking Log
QA Audit Form
Screening Log
Setting Up – Maintaining Study Files
Staff Signature Responsibility
Subject Enrollment Log
Study Management Checklist