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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UL Knowledge Services workshops are designed for and intended to serve individuals using and relying upon UL services. UL Knowledge Services reserves the right to limit workshop attendance strictly to the foregoing. In addition, UL Knowledge Services reserves the right to change, reschedule or cancel any workshop at any time. UL shall not be responsible for any consequential or other losses resulting from the cancellation or postponement of this workshop such as airline and other travel/personal expenses.
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