Wednesday 9th November, 2016
1:45pm to 2:30pm
With translation projects for products from strongly regulated industries like medical devices or pharmaceuticals, the requirements for the localization and translation of software, user manuals, instructions for use and also marketing materials differ in some important aspects from the ones for "traditional" technical translations. This session will give an introduction on the main areas to be taken into consideration when setting up a robust translation process for medicinal products.
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