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Fauls to Manage Regulatory Affairs at JenaValve Technology.

M2 PHARMA-January 8, 2016-Fauls to Manage Regulatory Affairs at JenaValve Technology


- US-based heart-valve technology company JenaValve Technology, Inc. has appointed veteran medical device executive Janet M. Fauls as vice president of regulatory affairs, the company said.

Fauls, who has nearly 30 years of regulatory and clinical affairs experience, will be based at JenaValve's corporate headquarters in Irvine, California.

Most recently, Fauls served as vice president of global regulatory affairs for Endologix, Inc. in Irvine, California.

Prior to Endologix, Fauls held management positions of increasing responsibility in regulatory and clinical affairs positions at major global medical technology companies including Edwards Life Sciences, Cardiogenesis Corp. and Allergan, Inc. Fauls earned B.S. in Chemistry from the University of California at Santa Barbara.

JenaValve Technology, with operating locations in Irvine, California, Leeds, England and Munich, Germany, develops, manufactures and markets transcatheter aortic valve replacement systems to treat a broad spectrum of patients suffering from aortic valve disease.

The company's Transapical TAVR system, consisting of the JenaValve valve system plus Cathlete PLUS delivery system, has CE Mark approval for aortic valve stenosis and for the unique indication to treat patients suffering from aortic valve insufficiency.

JenaValve currently markets this product in Europe and other selected markets worldwide. JenaValve is backed by US, European and Asian investors.

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Publication:M2 Pharma
Geographic Code:1U9CA
Date:Jan 8, 2016
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