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2011 Webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

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The document summarizes a live webinar on medical device regulations in the EU. The webinar will discuss EU directives, guidance documents, the CE marking process, and ISO certification requirements for commercializing medical devices in Europe. Attendees will learn about classifying devices and the regulatory requirements for approval and marketing in the EU. The webinar leader has over 27 years of experience in medical device regulation in Europe and globally.

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2011 Webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
2011 Webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
2011 Webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

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