Documents & Templates
Hands-on resources for clinical research including checklists, templates, SOPs, and tracking sheets
Close-Out Visit Checklist
Guide site close-out activities systematically, ensuring all regulatory and data requirements are finalized before study completion.
Routine Monitoring Visit Checklist
Ensure thorough and consistent routine monitoring visits with this comprehensive CRA checklist covering all essential review areas.
Pre-Study Site Assessment Checklist
Systematically evaluate potential clinical trial sites for capabilities, resources, and regulatory compliance before study start.
Informed Consent Documentation Review Checklist
Verify informed consent documentation completeness and compliance with this detailed review checklist for monitors and auditors.
Essential Documents TMF Review Checklist
Ensure Trial Master File completeness and audit readiness with this systematic review of ICH GCP essential documents.