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Highlighted Event

The European Medical Devices Regulation

The European Medical Devices Regulation

27 - 28 January 2015

The European Parliament has now completed their examination of the proposed regulations and has voted on their proposed amendments. With changes imminent, now is the time for industry to plan for the challenges ahead. Informa Life Sciences’ The European Medical Devices Regulation will include in-depth analysis of unannounced audits and joint audits of Notified Bodies, the changing responsibilities of economic operators, Medical Device classification and reclassification and the role of the Qualified Person.

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