Documents & Templates

Hands-on resources for clinical research including checklists, templates, SOPs, and tracking sheets

Resources

Subcategories

Guide site close-out activities systematically, ensuring all regulatory and data requirements are finalized before study completion.

Ensure thorough and consistent routine monitoring visits with this comprehensive CRA checklist covering all essential review areas.

Systematically evaluate potential clinical trial sites for capabilities, resources, and regulatory compliance before study start.

Verify informed consent documentation completeness and compliance with this detailed review checklist for monitors and auditors.

Ensure Trial Master File completeness and audit readiness with this systematic review of ICH GCP essential documents.