Simplify regulatory compliance and improve efficiency.
Our eTMF (Electronic Trial Master File) web-based system helps to streamline the trial process and ensure that all relevant information is readily available to relevant stakeholders.
Management of your clinical studies documentation
As regulatory requirements continue to evolve managing clinical trial documentation has become an increasingly critical and complex process.
With our eTMF solution, you can efficiently replace paper-based processes and manual document handling. Our secure and user-friendly platform enables seamless collaboration, simplifies audit trails, and ensures compliance with regulatory standards.
Whether you're conducting clinical trials, managing research data, or overseeing regulatory submissions, eTMF provides the tools you need to stay ahead.
With our eTMF solution, you can efficiently replace paper-based processes and manual document handling. Our secure and user-friendly platform enables seamless collaboration, simplifies audit trails, and ensures compliance with regulatory standards.
Whether you're conducting clinical trials, managing research data, or overseeing regulatory submissions, eTMF provides the tools you need to stay ahead.
Key features
By implementing our solution, you can transform your document management process, saving time, reducing errors, and increasing overall efficiency.
Easily manage document versions, revisions, and access history.
VERSION CONTROL AND DOCUMENT TRACKING
Facilitate collaboration among team members, assign tasks, and track progress.
COLLABORATION AND WORKFLOW MANAGEMENT
Store all your trial documents in one secure and accessible location.
Stay compliant with regulatory requirements and simplify audit preparations.
CENTRALIZED DOCUMENT REPOSITORY
COMPLIANCE AND AUDIT READINESS
Quickly find the documents you need using powerful search capabilities.
Ensure data confidentiality and control user access with role-based permissions.
ADVANCED SEARCH AND RETRIEVAL
DOCUMENT SECURITY AND ACCESS CONTROL
Designed to accommodate the evolving needs of organizations handling multiple trials. It can integrate with regulatory submission platforms allowing for direct transfer of trial documents.
SCALABILITY AND INTEGRATION
© 2024 Promeditec Innovation S.r.l.
Via dell'Orologio, 6
34121 Trieste
(+39) 040 2457504
info@promeditec.com
Via dell'Orologio, 6
34121 Trieste
(+39) 040 2457504
info@promeditec.com