Medical Devices Directives: Lessons Learned and the Way Forward

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Starts:  Thu, Nov 18, 2010 (CET)
Ends:  Fri, Nov 19, 2010 (CET)
The revised MDD 93/42/EC (via 2007/47/EC) took effect in March 2010, marking the onset of more rigorous regulations to which medical device manufacturers must adhere while addressing competitive market pressures, emerging technologies and higher patient expectations. Regulatory professionals in this space are responsible for their companies’ compliance with current regulations as well as developing and executing successful business strategies around revisions that directly impact the bottom line and their companies’ abilities to operate.
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Brussels

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