Clireo eTMF



Features Overview

arivis’ electronic Trial Master File solution - Clireo eTMF - enables companies to easily demonstrate compliance and control over their clinical document processes. Clireo eTMF allows companies and their external users (vendors, CROs, consultants, sites etc.) to securely review, audit, inspect, and search TMF documentation from any location in accordance with ICH and 21 CFR Part 11 guidelines.

How it works

Clireo eTMF is an out-of-the-box, cloud-based, solution that includes repositories defined in the Drug Information Association's best practices for Clinical Electronic Trial Master Files (DIA eTMF Reference Model).

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Clireo eTMF is supported by a complete cloud-based document management system to facilitate any eTMF business process. Clireo eTMF includes inspector portal, workflow, version control, document staging areas, FTP connectivity, and a full standards-based API. Easily add Clireo eCTD for global regulatory e-submissions.

Clireo is easy to use and is supported by one of the friendliest and cost effective licensing models amongst eTMF software providers.

In addition to software, arivis provides comprehensive professional services encompassing everything related to your TMF. arivis focuses exclusively on the Life Sciences and has deployed eTMF solutions for companies large and small. It’s time to consider the best solution for your eTMF - that solution is Clireo eTMF.