Your Pathway to Accelerated Trials and Streamlined Trial Master
File (TMF) Management
Rapid Deployment
Our pre-built models and configurable structure can significantly reduce setup time compared to building a system from scratch. It can be set up over a span of 2 weeks which translates to a faster deployment and minimizes disruption to your workflows.
Easy-to-use Interface
Find what you need quickly, even with complex studies. Clinion electronic trial master file (eTMF) software utilizes pre-built DIA TMF Reference Models and configurable organization-specific models. This translates to a well-organized system that allows for intuitive document filing and retrieval.
Complete Control and Real-Time Oversight
Automated version control and live tracking of missing documents empower you to maintain complete control over your trial master file (TMF). Gain real-time insights into document status and completion rates, ensuring a compliant and inspection-ready TMF at all times.
Safety and Compliance at the Forefront
Clinion eTMF software prioritizes safety and compliance with features like electronic signatures and audit trails. These features reduce the risk of human error and simplify regulatory audits by providing a clear and traceable record of all TMF activity.
Powerful Features
Supercharge Your trial master file (TMF) with advanced functionalities like pre-built models, configurable structure, real-time tracking, and advanced analytics to optimize processes, ensure ongoing compliance, and make data-driven decisions.
The Next Gen Trial Master File (TMF) Management for
Real-time Inspection Readiness
Our eTMF system has unique features that make storage, access and management easier. The simple user-interface makes it the go-
to tool for clinical trial document management.
Want to Experience Next Gen TMF Management?
