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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.
"Very good, interesting talks and interactive exhibition"
"One of the major meetings in the market"
"Professionals in academia, industry and governments should attend this yearly update in vaccinology."