This webinar will provide valuable assistance and guidance to all regulated companies that are preparing for CE Mark and ensuring compliance to MDD 93/42/EEC.
Medical Devices in the EU: CE Mark and 93/42/EEC Directive
16 September 2010, Palo Alto, United States
Introduction
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Online Event
Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
Organised by
ComplianceOnline
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