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HealthLink Europe's U.S. Operation Supports First FDA IDE Trial
Date:11/11/2013

RALEIGH, N.C. and 'S-HERTOGENBOSCH, Netherlands, Nov. 11, 2013 /PRNewswire/ -- HealthLink Europe, an ISO 13485:2012 certified company specializing in providing front and back office support, VAT deferment, fulfillment and logistics services to medical device companies since 1994, is now supporting a European-based client's FDA IDE Trial in the United States for a Class III device in the interventional cardiology space.

HealthLink Europe has had a Business Development and Client Relations office based in Raleigh, North Carolina since 2004, but they have now expanded their North American capabilities to include logistical support. HealthLink's expansion of operational services to the U.S. offers its current clients the advantage of working with the same platform for their sites in the U.S. as they do for their European operations.

HealthLink plans to grow its North American warehousing and logistics services with the expansion of its U.S. team based in Raleigh, North Carolina. Sebastiaan "Bas" de Kok, Operations Manager at HealthLink Europe, will join the U.S.A. team this year, bringing with him the knowledge and experience necessary to further develop HealthLink's North American endeavor.

"It is our plan to have a North American operation that offers similar services to our current European facility in the Netherlands," explains Rick Hughes, president of HealthLink Europe. "We're very excited about our expansion and we're looking forward to supporting our clients as they expand into other markets."

ABOUT HEALTHLINK EUROPE:
HealthLink Europe is 100% medical, ISO 13485 certified, specializing in class II and III devices and their associated regulatory re
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SOURCE HealthLink Europe
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