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AxxiTrials.com
Axxcelerate Your Trials

Clinical Trials Portal Solution

Litéra AxxiTRIALS, a secure portal solution that speeds trial operations processes from Feasibility to Close-Out, help complete studies on time, on budget and with the quality of data required.

Litéra AxxiTRIALS reduces trial start-up and operations management staff time by approximately 65% on average throughout the life of the trial by automating feasibility survey management, document exchange and signature, trip reporting, communication, training, safety alerts, task tracking, status reporting and archiving processes - all in one system that integrates with existing systems.

At the clinical research sites, AxxiTRIALS reduces time spent by PIs and study site coordinators so much, site adoption averages an unheard of 90% or more. As a single touch point for all the trial’s content and systems, sites can easily complete feasibility surveys, regulatory document submission, elearning, safety alert acknowledgement and more. AxxiTRIALS' streamlined interface is so intuitive, sites can use it immediately with no training, but they can also securely email their documents directly into the portal without even logging in! Site engagement is increased with leaderboards, community tools, live access to CRO staff and more.

Finally, all sponsors want transparency into the status of their trials and today some are seeking self-serve. Litéra AxxiTRIALS is the only portal that delivers real-time reporting of all KPIs, including leading and lagging indicators in a graphical snap-shot view, with drill-down to whatever level of detail they desire.


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The leading automated RegDOC exchange and workflow portal announces

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Announcing AxxeTMF

The simple, cost effective, fully automated eTMF solution

AxxeTMF is unique because it leverages an Automated Rules-based Engine to automatically:
  • Distribute - Determines what documents and metadata are expected from whom and distributes requests
  • Remind - Sends reminders for missing items
  • Collect - Collects documents and metadata
  • Route - Routes for review and approval
  • File - Names and files based on the associated artifact
  • Report - Reports status in real time
    On average:
  • 35% of eTMF documents are collected with no staff involvement whatsoever, reducing costs and chance for manual error significantly
  • Documents are received within 21 days, accelerating the trial, especially study site activation
  • Simple interface results in site adoption of as much as 91% with little or no training on how to use the portal, reducing staff workload.
 
AXXCELERATING Clinical Trials

 
 
 
The AxxiTRIALS Feasibility Module

  From the Site's perspective
  From the CRO/Sponsor's perspective

Key Features

  • Survey Tool: full feature custom survey tool
  • Survey invite system with automated login information included
  • Data prepoplate functionality
  • Automated Reminder System
  • Robust reporting with drill down for details
  • AxxiTRACKER, site level reporting and tracking tool included!