New European Regulations Demand Medical Translation For Medical Devices & Pharmaceuticals

FOR IMMEDIATE RELEASE
(Free-Press-Release.com) September 14, 2009 -- New European Union regulations require that all packaging and instructions for medical devices and pharmaceuticals be translated into the native language of the importing region.

If American companies wish to market to European medical device and pharmaceutical customers, they must provide this translated documentation in order to remain competitive with their European counterparts.

THE MARKETING ANALYSTS have over 20 years of experience providing medical translations for medical device and pharmaceutical companies doing business in Europe. Among our many satisfied high-profile customers are major pharmaceutical companies in the USA, Germany, Belgium and Switzerland, and medical device companies in the USA, France, Germany, Switzerland and Austria.

Read More on Medical Translation: http://www.themarketinganalysts.com/en/pages/medical-translation-interpretation-pharmaceutical-equipment-specifications-medical-literature-hippa/

THE MARKETING ANALYSTS can help you sort through the many EU regulations regarding translations of medical documentation, and guarantees your 100% satisfaction. What’s more, our rates are much more affordable that those of our European competitors since we are not required to charge Value Added Tax, which can add up to 20% to your total translation cost. We also pledge to meet or beat our competitors‘ pre-tax rates on translations.

More information can be found online at http://www.themarketinganalysts.com/en/pages/medical-translation-interpretation-pharmaceutical-equipment-specifications-medical-literature-hippa/

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