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EMD Serono to Adopt Revised and Strengthened PhRMA Code
Date:7/10/2008

r and develop and we remain committed to informing healthcare professionals about the company's therapies and research programs. The ability to provide physicians with timely, accurate medical and scientific data regarding our medicines is of the utmost importance, to help ensure proper patient care.

"As the team responsible for EMD Serono's compliance oversight we look forward to implementing the revised Code, continuing our strong compliance training programs for employees and are very pleased to have participated in the development of the new Code," said Robert Freeman, Chief Compliance Officer of EMD Serono, Inc. "It remains paramount to our organization that our interactions with healthcare professionals meet the highest ethical standards while delivering valuable information to healthcare professionals and patients."

EMD Serono is one of a few biopharmaceutical companies with US headquarters in the state of Massachusetts that is a member of PhRMA. EMD Serono remains a leader in conducting ethical interactions with healthcare providers to ensure patients can obtain the products necessary to treat their illnesses appropriately.

Additional information on the revised code can be seen at http://www.phrma.org

About EMD Serono, Inc.

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, is a leader in the US biopharmaceutical arena, integrating cutting-edge science with unparalleled patient support systems to improve people's lives. The company has strong market positions in neurodegenerative diseases, with Rebif(R) (interferon beta-1a), as well as in endocrinology, with Saizen(R) (somatropin (rDNA origin) for injection), Serostim(R) (somatropin (rDNA origin) for injection) and Zorbtive(TM) (somatropin (rDNA origin) for injection). EMD Serono is a leader in fertility treatments, with Gonal-f(R) (follitropin alpha for injection), Luveris(R) (lutropin alfa for injection) and
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SOURCE EMD Serono, Inc.
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