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   Topics to be Addressed:
Global Harmonization efforts, ongoing impact of the Medical Device Directive recast, legal & reimbursement perspectives, IEC 60601 3rd compliance, trends on clinical review, overcoming regulatory hurdles throughout the European, USA, Brazilian and China market, opportunities in meeting notified bodies, Medical technology management and more! Our Qserve International Conference on November 14 & 15, 2011 has been pre-approved by RAPS as eligible for up to 12 points towards a participant’s RAC recertification upon full completion.
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