At Docutrial, we are revolutionizing the way you capture and process clinical trial data.  The Docutrial electronic platform is the next generation of paper-free platforms for managing clinical trial data and document management.  

Docutrial is an affordable and intuitive platform for eSource, CTMS, eISF, eReg and EDC and has been used in over 300 studies including studies from most major pharma companies. 

The Docutrial platform dramatically improves efficiency and reduces costs for:

▪️ Sites
▪️ Contract Research Organizations (CROs)
▪️ Sponsors.  

HOW IT WORKS 

Used in over 300 studies including most major pharma companies, Docutrial uses electronic tablets, scanning, and electronic file storage. Each site has its own source documents and forms, but entry is done on an iPad or tablet with a digital pencil. All notations are then instantly captured and converted into usable data so you can monitor completed source documents instantly and in real time- not weeks later. This enables more efficient remote monitoring, reduces travel expenses, and simplifies the query process. 

Docutrial is certified to meet FDA regulations and ICH Good Clinical Practice Guidelines. All source documents are backed up on the device as well as in the cloud, protecting against potential data loss.  

THE DOCUTRIAL DIFFERENCE 

What makes Docutrial different is you have one platform that captures all data for eSource, CTMS, eReg, eIsf, and EDC which can be accessed anytime and from any device. The simplicity of our platform eliminates data re-entry and makes it easy for a CRO to provide Docutrial to sites instead of a more cumbersome EDC system.  

And for sponsors, faster data means faster FDA submission. 

So if you’re struggling with getting and verifying data and finding the manpower to do it, reach out, and we’ll help you eliminate paper entry, increase efficiencies, and dramatically reduce overhead at your sites.  

See our website for a full demo of Docutrial.

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