Clinical Trails involve lot of patients, sites, systems, etc. generating huge data throughout the process. In order to efficiently manage the trails, MFPL has developed its own Clinical Trial Management System (CTMS) with an integrated Electronic Trial Master File (eTMF) solution to consolidate all trial data. MFPL CTMS is an end-to-end clinical trials management solution that brings control, efficiency for both data flow and workflow, and quality data to every study within affordable cost, time and operational expenses. Our eTMF clinical trial software is a solution that can get up and running quickly and efficiently. Built on the same platform as MFPL CTMS and available with affordable add-on pricing, it meets all regulatory requirements, from support for the most recent DIA Reference Model to 21 CFR Part 11 compliance to a complete audit trail.
It allows organizations to define their own / Sponsor specific TMF structure and milestones along with live tracking of missing documents. It is one of the best eTMF software which has a robust document lifecycle with Author, Review, eSign/Approval workflow & Automated version controlling with robust Check-in and Check-out functionality. Our systems allows bulk and quick uploading including sharing and collaboration of documents across the systems. Our systems are feature rich and flexible which provides easily configurable workflows to meet the Sponsor SOPs and every requirement of clinical trials. Our systems are powerful with the best actionable dashboards and reports for real time monitoring and tracking of study and site statuses which are user-friendly and can be accessed with any internet browser.
With Microsoft-office based environment, both the systems deliver easy and seamless exchange to Sharepoint or Microsoft products. The systems are easy to learn and use, making it’s adaption quickly for the end user. This web-based CTMS and eTMF clinical trial software works in a way to help Sponsor to view and manage real-time operational performance.