Electronic Trial Master File Management
The PharmaReady TMF Consulting team can provide strategic planning and support in implementing an electronic centralized method of compiling, storing and archiving the TMF documents. PharmaReady Document Management System is equipped with customizable Trial Master File Templates that capture searchable document metadata enabling instant access to all the stake holders and document owners of the Trial Management.
The PharmaReady TMF Consulting team is highly qualified to assist sponsors to organize and implement Trial Master Files to demonstrate the compliance of the investigator, sponsor and monitor with the standards of GCP and with applicable regulatory requirements. We provide guidance to file documents in an organized way that will facilitate management of the clinical trial, audit and inspection.