| Medical Device Consultants Inc. Press Release |  |
MEDICAL DEVICE CONSULTANTS, INC. PARTNERS WITH FOREIGNEXCHANGE TRANSLATIONS
Industry leaders unite to provide medical device manufactures with seamless global service offerings
Medical Device Consultants, Inc. (MDCI), a worldwide provider of regulatory consulting and clinical research services exclusively for the medical device and in vitro diagnostics industries, announced that it has entered into a strategic partnership with ForeignExchange Translations, Inc., a leading provider of multilingual compliance solutions to the medical device industry.
"ForeignExchange Translations has earned the respect of many industry leading medical device manufacturers," said Bill Morton, CEO and founder of MDCI. "We are enthusiastic about our partnership with ForeignExchange Translations. Together we can deliver turnkey translation and regulatory services for our client and prospects. Presently this is especially valuable to IVD product manufacturers who are working to obtain the CE Mark for their products."
Both firms work closely with industry-leading medical device manufacturers. "We are excited about our partnership with MDCI," said Andres Heuberger, President of ForeignExchange Translations. "Our clients often run into regulatory challenges when preparing their translation strategy for entry into global markets. MDCI's expertise in navigating Europe's Medical Device Directive will serve our current and future clients extremely well."
MDCI has offices located in North Attleboro, MA, San Diego, CA, Raleigh, NC, London, England and Paris, France. ForeignExchange Translations has offices in Cambridge, MA, Providence, RI and Louisville, CO, with partners and affiliates throughout Europe and Asia.
About Medical Device Consultants, Inc.
Medical Device Consultants, Inc. (MDCI) provides regulatory, clinical, and QA consulting services to IVD manufacturers for developing and implementing worldwide regulatory strategies to meet US FDA, Canadian, and European requirements. Services include: strategic planning, regulatory submissions, CE marking, EC Authorized Representative, U.S. Agent, multinational clinical studies, data management, and quality system design, implementation and assessment. For more information visit www.mdci.com.
