Quality First International

Transposition of Amending Directive 2007/47/EC Medical Devices

Various practical matters require attention in order for a medical device manufacturer to be able to declare conformity to Amending Directive 2007/47/EC in time to fulfil the period of transition, where applicable.

Complete the short form below to access a FREE white paper on this topic, which has been written by Haroon Atchia, CEO and Technical Director of Quality First International:

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