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eTMF solutions & documentation
eTMF solutions & documentation
Artialis will ensure preparation and management of all essential clinical documentation needed to support your clinical trial. It includes :
Study synopsis, protocols and protocol amendments
Patient information letter and Informed consent form
Site logs and forms
Subject questionnaires
All study plans including Project management plan and associates plans as monitoring, TMF, etc.
Study reports and CSR
Certified translation of any patient document
Artialis is using trial Interactive eTMF to collect and store documents of your clinical trial. Your trial data will be kept safe in a password-protected environment during your trial. You will have direct access to any of your trial documents. We will create a TMF plan, and upload and manage documents to ensure consistency, accuracy, and readiness until trial closure and archiving.
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