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QIAGEN Receives Regulatory Approval in Japan for EGFR Companion Diagnostic to Guide Cancer Treatments
Date:1/9/2012

ls, 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 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).Contacts:Investor RelationsPublic RelationsJohn Gilardi

+49 2103 29 117
+1 240 686 2222

Dr. Thomas Theuringer

+49 2103 29 11826
+1 240 686 7425Albert F. Fleury

+1 301 944 7028
IR@qiagen.com

Brendan Green

+86 21 3865 3824
PR@qiagen.comwww.qiagen.com/about/investorrelation

www.qiagen.com/about/press
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