Monday, 29 October 2012

Implementing new directives and standards in practice

The Medical Devices Directive (MDD) is currently undergoing comprehensive revision by the European Commission.At MEDICA 2012 (Hall 10, Stand B05) TÜV SÜD will inform medical devices manufacturers of how the changes will affect the harmonized standards and how requirements can be implemented in practice.The MEDICA trade fair will take place in Duesseldorf between 14 and 17 November.

To read the full article, please click HERE.
 

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