| Medical Device Consultants Inc. Press Release |  |
MDCI Welcomes Leslie Rose as Director, Clinical Project Management
North Attleboro, MA, July 7, 2008 - Medical Device Consultants, Inc. (MDCI), a leading regulatory consulting firm and CRO for the medical device industry is pleased to welcome Leslie Rose as Director, Clinical Project Management.
"As we support more and more medical device developers and manufacturers who are bringing innovative and cutting-edge medical device products to market, we've seen an expansion in the size, scope and complexity of clinical trials to support their products", said Michael Feldstein, Vice President of Clinical Services. "Leslie brings a proven ability to build and motivate high performing teams, along with extensive experience in the planning and execution of medical device clinical trials, which will serve both MDCI and our clients extremely well."
Leslie brings over sixteen years of medical device industry and clinical research experience, from her roles at companies such as Haemonetics Corporation and Dade Behring, (now part of Siemens Healthcare Diagnostics). She will oversee MDCI's clinical project management teams to develop and conduct medical device clinical trials that will support and align clients' business and regulatory requirements. Leslie is particularly knowledgeable in the areas of blood processing equipment and in vitro diagnostic products.
Leslie holds her M.S. in Clinical Laboratory Science from the University of Rhode Island and B.A. in Biochemistry from Mount Holyoke College.
About MDCI
MDCI is a full-service consulting firm and contract research organization (CRO) that helps emerging and established firms commercialize novel and innovative medical devices, in vitro diagnostics, and combination products. Clients trust MDCI to deliver customized strategic guidance and creative "hands-on" solutions to address their unique regulatory, clinical trial, and quality assurance challenges at every stage of the product lifecycle.
MDCI has helped hundreds of clients conduct successful clinical trials, achieve regulatory clearance and approval, and maintain compliance for products in the U.S. and internationally. By leveraging our comprehensive knowledge of FDA and international regulations, clients capture and grow market share, increase productivity, and stay competitive in an increasingly complex global marketplace.
Visit www.mdci.com or call 1 508 643-0434 for more information.
