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	Thanks to the European Union's (EU) Medical Device Directive (93/42/EEC) (MDD), medical translation services have crossed over from a useful option to a must-have solution for many businesses in the medical field. Medical manufacturing companies now realize that English does not have a monopoly on the industry any more. This Directive requires medical firms to adopt a specific multilingual documentation process. This effectively creates the need for these firms to make specific provisions for translation of such documents as product packaging, end-user instructions and labels, among others. And while previous directives may have specified that certain languages should be used for medical information, this MDD makes it a definite and absolute requirement.

Of particular note for the translation industry is MDD 93/42/EEC Directive Annex I Article 13.1 which states that "each device must be accompanied by the information needed to use it safely and to identify the manufacturer, taking account of the training and knowledge of the potential users."

Considering that product information falls into professional and patient use classifications, localization of informational material particularly for medical non-professionals must be as precise and understandable as possible in any given language.

Manufacturers will often use in-house assets for medical translation purposes. However, this often results in poor translations, which of course can result in serious legal issues for the company in question. Outsourcing to localization companies that offer expert medical translation services can help companies follow the EU MDD 93/42/EEC Directive as closely as possible, while saving on personnel and project management costs as well.

Article Source: http://EzineArticles.com/4928852

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