March 26, 2007 09:32 ET

Compliance Leader QUMAS Exhibiting at RAPS 2007 Horizons Conference & Exhibition

FLORHAM PARK, NJ -- (MARKET WIRE) -- March 26, 2007 -- QUMAS, a leading provider of quality management and regulatory affairs solutions, today announced that it is exhibiting at the RAPS 2007 Horizons Conference & Exhibition March 28 - 30, the Palace Hotel in San Francisco. QUMAS will be located at table #32 in the Grand Ballroom.

Encompassing international perspectives and understanding of the global regulatory environment, the RAPS 2007 Horizons Conference & Exhibition brings together Regulatory Affairs (RA) professionals and experts for an interactive global forum. Industry leaders, key FDA personnel and international regulatory affairs professionals address pertinent issues impacting FDA-regulated companies and provide RA professionals the tools they need when bringing new products to market, entering emerging markets and planning for the future.

QUMAS representatives will be in attendance to discuss and demo its QUMAS Compliance Suite™, a complete compliance framework that allows life sciences firms to initiate enterprise-wide compliance management programs that cover many regulations with a single solution. In particular, QUMAS representatives will be on hand to discuss how companies can accelerate business processes, reduce costs and improve quality in the midst of changing and new regulatory policy initiatives that impact pharmaceutical companies' ability to bring drugs to market in the near term.

In addition, QUMAS will be featuring the QUMAS R&D Suite, a comprehensive, integrated solution for organizations looking for an all-inclusive content management and publishing system. The QUMAS R&D Suite eliminates the need for companies to go out and assemble an R&D solution on their own. This approach saves valuable time, resources, costs and complexity in managing the solution over time.


QUMAS is a leading developer of enterprise compliance management solutions designed to help life sciences organizations meet industry and government standards for 21 CFR Part 11, cGxP, Quality, Regulatory Affairs and Clinical Operations. With over a decade of experience, QUMAS is helping companies accelerate business processes, reduce costs and improve quality. From content lifecycle management, business process and change management to reporting and analysis, QUMAS Compliance Suite is successfully enabling global life science organizations to proactively manage their regulated content and processes in a secure and compliant way.

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