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The Changing Regulatory Landscape for In Vitro Diagnostics


Description

The purpose of this webinar is to highlight the significant changes taking place in the In Vitro Diagnostics (IVD) regulatory world over the next 2 to 3 years.  This seminar provides a preview of these changes to help customers consider how their business might be impacted and to start planning for how they accommodate these changes within their systems.  The process of revising the directive started in the summer of 2010 when the European Commission launched a public consultation exercise on modernizing and updating the current IVD regulations. This exercise involved representatives from the industry as suppliers, from health care institutes as users, and from regulatory bodies and other concerned individuals.  A large degree of consensus that has been reached and draft recommendations of each will be published in the autumn of 2012.

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Media

Time Requirement

Cost

Web-Based 40 minutes $99.00
 









 
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