Centralized eTMF That Keeps Your Studies Inspection-Ready
Our eTMF solution provides a centralized, easy-to-use platform that streamlines the organization, tracking, and compliance of your Trial Master File (TMF) — helping sites and study teams stay on schedule and prepared for inspection. With real-time visibility into essential trial documentation and automated, compliance-focused workflows, you can reduce manual effort, eliminate bottlenecks, and maintain documentation quality across all your studies.
Efficient document management
Upload, organize, and retrieve files quickly with bulk upload capabilities and intuitive folder structures. Visual dashboards and real-time tasks lists make it easy to track documentation and actions across studies and teams.
Real-time compliance insights
Identify overdue or missing documents with visual indicators and automated alerts. Built-in quality checks and global compliance frameworks help ensure documentation accuracy and regulatory readiness.
Audit-ready at every step
Maintain a complete audit trail with timestamped actions, review histories, and secure document storage to support inspections with confidence.
Automated review and signatures
Accelerate documentation workflows with configurable review processes and electronic signatures.
Streamlined collaboration across teams and sites
Enable seamless collaboration between sponsors, CROs, and investigative sites with an eTMF that works for both trial team and site documetation. Teams can access current documents, submit updates, and track progress from a single system — reducing silos and duplicated effort.
Upholding the Highest Compliance Standards
Contact us for an introduction to Mednet's comprehensive EDC-centric eClinical platform with key native modules to support all study types and phases – such as randomization, trial supply management, adjudication, ePRO, payments, DICOM imaging, eConsent and more.