Electronic Trial Master File (eTMF)
The GLOBAL CRO Approach
An eTMF allows you to digitally capture, manage, share, and store trial-related documents from a clinical trial. It is critical that eTMF are designed strategically to ensure adherence with good clinical practices (GCP), and meet regulatory requirements while maintaining an acceptable level of detail and quality. A streamlined eTMF can save you money and monitoring costs by keeping all documents stored and updated throughout the trial life cycle.
Our Services Include:
eTMF System Administration
Active eTMF Management
Governance and Quality Assessments
Why Choose GLOBAL CRO?
GLOBAL CRO leverages years of experience and cutting-edge technology to design and deliver customized eTMFs that ensure complete trial documentation and organization. We can work with your preferred eTMF vendor or can offer a robust application at an affordable rate. From design to implementation, GLOBAL CRO combines clinical and technical experience to customize an eTMF that can accommodate unique requirements from early feasibility to pivotal and post market trials.