SOURCE: QUMAS

January 22, 2008 08:00 ET

QUMAS Compliance Expert Sean Winslow to Speak at 21st Annual DIA Conference for Electronic Document Management

QUMAS to Feature R&D Solution in Booth #402

JERSEY CITY, NJ--(Marketwire - January 22, 2008) - QUMAS, the leader in Enterprise Governance, Risk and Compliance (GRC) solutions, today announced that Sean Winslow, manager of global implementation consulting and professional services, will speak on "Redesigning the EDMS: Turning Lessons Learned into a New Streamlined Benefit" at the 21st Annual DIA Conference for Electronic Document Management. Winslow's presentation will be on Friday, February 8 from 10:30 a.m. to noon at the Philadelphia Marriott Downtown in Philadelphia, Pennsylvania.

Winslow brings his experience and domain expertise to the Conference, having implemented and re-implemented enterprise compliance systems in the life sciences industry for nearly a decade. His presentation will focus on configurations that offer life sciences companies greater scalability and increased performance for optimal electronic document management. In order to realize these benefits, life sciences companies must be willing to re-examine how they approach document management and storage when setting out to tackle upgrades, migrations or redesign projects.

To illustrate his points, Winslow will cite real-life examples that drive a re-design decision. Other specifics include:

--  Project planning
--  Resource management
--  How to leverage the right people to ensure the most efficient process
    is followed
--  Resulting enhanced customer satisfaction
--  Cost benefits and ROI
    

In addition to Winslow speaking at the conference, QUMAS is a DIA exhibitor in booth #402. February 6th-7th, QUMAS will demonstrate its R&D Solution, designed to help life sciences companies bring new drugs to market quickly and cost-effectively within a secure and controlled environment.

The QUMAS R&D solution is an out of the box solution that assists life sciences companies in expediting the new drug application process with better quality submissions, fewer iterations, and shortened review and approval cycles for IND and NDA submissions. The R&D Solution has seen rapid adoption within the industry due to its best-of-breed software for:

--  Regulatory Content Management
--  Submission Management
--  Browser-based Collaboration
--  eCTD (electronic Common Technical Document) Authoring Templates
--  Import/Export Tool
    

For more information on the 21st Annual DIA Conference for Electronic Document Management, please visit http://www.qumas.com/news-events/events.asp.

About QUMAS

QUMAS is the leader in Enterprise Governance, Risk and Compliance (GRC) with more than 250 customer deployments and over a decade of experience helping companies in highly regulated industries provide a proactive regulatory defense.

QUMAS solutions for life sciences are designed to achieve compliance with industry and government standards for 21 CFR Part 11, cGxP, Quality, R&D, Regulatory Affairs and Clinical Operations. QUMAS enables organizations to bring new drugs to market faster with better quality submissions while proactively managing regulated content and controls, reducing costs, and improving customer satisfaction.

For more information visit http://www.qumas.com.

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