New Webinar: The Changes to CE Certification of Medical Devices Starting in 2014

MessageThis Webinar is over
Date Nov 13, 2013
Time 9:00 GMT+1
Cost Free
Online
AGENDA

Introduction and Background
Changes to Audits and Quality Management Systems
Unannounced Audits
Changes to Technical Documentation and Technical File Assessments
Changes for Notified Bodies
Changes to Contracts
Priority Actions for Manufacturers

TARGET AUDIENCE

Medical device manufacturers and organizations who have certification under one of the European medical device directives (Active Implantable Medical Devices, 93/42/EEC Medical devices and 98/79/EC In Vitro Diagnostic Medical Devices) or who plan to obtain such certification. Those people involved with or responsible for quality systems, regulatory affairs, product design, manufacture or clinical activities will find the subject relevant.

 


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