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QIAGEN Acquires Comprehensive Portfolio of Molecular Food Safety Tests
Date:5/25/2010

th and international operations (including the effects of currency fluctuations, regulatory processes and dependence on logistics), variability of operating results and allocations between business segments, the commercial development of the applied testing markets, personal healthcare markets, clinical research markets and proteomics markets, women's health/HPV testing markets, nucleic acid-based molecular diagnostics market, and genetic vaccination and gene therapy markets, changing relationships with customers, suppliers and strategic partners, competition, rapid or unexpected changes in technologies, fluctuations in demand for QIAGEN's products (including fluctuations due to general economic conditions, the level and timing of customers' funding, budgets, and other factors), our ability to obtain regulatory approval of our infectious disease panels, difficulties in successfully adapting QIAGEN's products to integrated solutions and producing such products, the ability of QIAGEN to identify and develop new products and to differentiate and protect its products from competitors' products, market acceptance of QIAGEN's new products and the integration of acquired technologies and businesses. For further information, refer to the discussions in reports that QIAGEN has filed with, or furnished to, the U.S. Securities and Exchange Commission (SEC).

    Public Relations               Investor Relations

    Dr. Thomas Theuringer          Dr. Solveigh Maehler
    Director Public Relations      Director Investor Relations
    +49-2103-29-11826              +49-2103-29-11710

                                   Albert F. Fleury
                                   Investor Relations North America
                                   +1-301-944-7028
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SOURCE Qiagen
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