Viedoc TMF is our fully integrated document management system—highly secure and with 24/7 accessibility. Based on industry standards and equipped with permissions, document review, and a customizable structure, Viedoc TMF makes documentation easier, smoother, and above all: faster.
With Viedoc TMF, all your trial documentation is at your fingertips, accessible from a single interface. Its powerful search engine feature easily locates any document in an instant.
Knowing that documentation is one of the most time-consuming parts of a clinical trial, we’ve made sure that Viedoc TMF provides everything you need in one place. End users can upload, access, review, approve and sign, lock documents from a single interface – with the same ease of use as the rest of the Viedoc suite.
As a TMF Manager, you can easily set up end-user permissions based on existing user roles. These permissions control the access that end users have on many levels.
As a Viedoc TMF client, you get access to our TMF template which is based on the DIA TMF Reference Model. And should you need to, Viedoc TMF’s easy configuration allows you to create your own structure exactly the way you want it.
Yes, all products in the Viedoc eClinical suite are fully 21 CFR Part 11 compliant.
Yes, everything in Viedoc eTMF is, of course, audit-trailed giving you the control you need over your trial—all in one suite.
Not at all; in Viedoc, you can create customizable structures to ﬁt the needs of any trial or organization.