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Aris Global, LLC Announces Release of Register 5.3


6/26/2012 12:35:59 PM

STAMFORD, CT—June 25, 2012—ArisGlobal, a leading provider of solutions to the life science industry, today announced the general availability of Register 5.3.

Register 5.3 is the latest version of ArisGlobal’s comprehensive, and proven regulatory e-submissions management and tracking solution used by 9 of the top 25 pharmaceuticals and life science companies across the world.

This release features enhancements to RegisterTM that allows users to manage the tracking of dossiers more efficiently and gives them the capability to better track and manage regulatory intelligence including supporting web links and documents, if any. These enhancements come with a user friendly field help feature that enables quick searching for very specific help with each field in the application.

“We are glad to announce the release of Register 5.3 in line with our track record of timely response to the rapidly evolving and converging global regulatory environment and the customer requirements that change accordingly. It is especially amazing that in a time in which all focus had to be on XEVMPD compliance that we have been able to introduce two new modules in our Total Regulatory solution. We believe that Register 5.3 will be a timely addition to the arsenal of companies looking to gear up for the big imminent change – ISO-IDMP,” said Wim Cypers, vice president for Regulatory Affairs at ArisGlobal.

The other updates for improved processing efficiencies include the ability to use multi-select criteria for a preferred product name, opening documents from query results, merging local updates, and improved tracking alerts.

RegisterTM 5.3 is available to customers immediately as a licensed, on-premise solution or as a hosted solution via agOnDemand™, ArisGlobal's comprehensive Software-as-a-Service (SaaS) delivery platform.

About ArisGlobal

ArisGlobal (www.arisglobal.com) is a leading provider of integrated software solutions for pharmacovigilance and safety, regulatory affairs, clinical research and medical information. Hundreds of life science companies rely on ArisGlobal’s advanced solutions for maintaining regulatory compliance, workflow automation, improving operational efficiency and easily sharing information around the globe.

Contact

Lorra Gosselin

ArisGlobal

+1.203.588.3000

lgosselin@arisglobal.com



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