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How the Medical Device Industry Can Prepare for the EU Regulatory Changes Ahead, New Life Science Webinar Hosted by Xtalks
Date:5/10/2013

Toronto, Canada (PRWEB) May 10, 2013

On 26 September 2012, the European Commission announced the release of a draft revision to regulations that will impact medical device and medical diagnostic manufacturers in the EU and abroad. These revisions will bring stricter requirements for clinical trial evidence and demand greater data quality. Is your organization prepared to comply?

Topics include:

  •     Requirements for clinical evidence
  •     Potential regulatory notification changes
  •     The emphasis on post market clinical follow up
  •     Class II devices and regulatory clinical investigations
  •     Tools available to support quality and compliance

For more information about this event or to register, visit: http://xtalks.com/EU-Regulatory-Changes-for-Medical-Devices.ashx

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks, visit http://xtalks.com/ContactUs.ashx.

Contact:
Karen Lim (416) 977-6555 ext 227
clientservices(at)xtalks(dot)com

Read the full story at http://www.prweb.com/releases/2013/5/prweb10718257.htm.


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