AxxiTRIALS announces the launch of AxxCELA™ and AxxCELA SEND™ at DIA 2017The regulatory document exchange solution for sites who are “log in averse.”
MCLEANSVILLE, North Carolina – June 16, 2017 – AxxiTRIALS, a secure portal solution designed to expedite clinical trial operations, is pleased to announce the launch of AxxCELA™ and AxxCELA SENDTM, tools to enable sites to submit their regulatory documents securely, efficiently and directly into the AxxiTRIALS automated workflow system without ever having to log in.
“With its customizable workflow engine, AxxiTRIALS is known for accelerating the regulatory document exchange process,” says Karen Massand, Managing Director of AxxiTRIALS. “Now, with AxxCELA, we make it even easier for sites to kick off that process by submitting their documents directly into the system, further reducing costs and raising efficiencies for Sites, CROs and Sponsors.”
AxxCELA SEND leverages industry-leading security technology to evaluate inbound email and process it through established security protocols. Files are then loaded into the AxxiTRIALS portal, metadata added and the assigned CRO/Sponsor staff member notified that the file is ready for their review.
The staff member simply clicks a link that takes them to the AxxCELA Matchmaker™ tool, where they can quickly and easily drag-to-match the file to an open action item. This kicks off the AxxiTRIALS workflow process, which automatically routes the document to appropriate people at the CRO and/or sponsor for approvals, tracks the document’s progress, updates reports, stores the document in the site’s eBinder and tags it for eTMF filing.
AxxCELA’s site-friendly approach significantly increases site adoption and speeds processing, resulting in reduced time to initiation and reduced costs.
AxxiTRIALS will officially launch AxxCELA at DIA 2017, June 18-22 at McCormick Place in Chicago, IL. Come see AxxCELA in action at booth #2623.
About AxxiTRIALS
AxxiTRIALS speeds clinical trial operations from Feasibility to Close-out, allowing studies to complete on time and on budget with the required quality of data. As a secure portal, AxxiTRIALS reduces trial start-up and operations management time throughout an entire project by automating tasks such as reports, alerts and archiving processes. AxxiTRIALS reduces time spent at clinical research sites by PIs and study site coordinators by simplifying their technology experience with a single solution for all trial content and systems. With leaderboards, community tools, and live access to CRO staff, AxxiTRIALS increases site engagement for internal staff. AxxiTRIALS is the only portal to deliver real-time reporting of all KPIs, including a snapshot view of all leading and lagging indicators for full transparency into the status of sponsored trials.
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