Key Changes to Medical Devices Directive 93/42/EEC – Webinar Recording
Key Changes to Medical Devices Directive 93/42/EEC – Webinar Recording
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Webinar Recording
This presentation goes through the key changes to Medical Devices Directive 93/42/EEC as a result of Amending Directive 2007/47/EC, as well as the challenges facing medical device manufacturers. It will then 
guide you through the steps required to meet the deadline of the 21st March 2010 for implementation of the changes.
This webinar will be beneficial to anyone involved with Quality, Regulatory and Marketing of medical devices within Europe, including senior management.
From listening to this webinar you will receive guidance from the leading medical device Notified Body to help you understand the changes and prepare to implement them. Please note that any products (including their labelling & instructions for use) that are non-compliant with the changes on the 21st March 2010 (even if manufactured before this date) cannot beplaced onthe market.
To request a copy of the presentation slides from this webinar, please click here.
Published 17th December 2009
