SOURCE: Xtalks

Xtalks Webinars

July 10, 2015 07:00 ET

he New EU Clinical Trials Regulation: What You Need to Know Before 2016, New Webinar Hosted by Xtalks

TORONTO, ON--(Marketwired - July 10, 2015) - This presentation on the new EU clinical trials regulation will identify what's happening with the regulation that governs clinical trials in Europe. Join featured speaker Dr. Martine Dehlinger-Kremer, Global VP of Medical and Regulatory Affairs at SynteractHCR, for a one-hour live session on Thursday, July 23, 2015 at 11am EDT (4pm BST/ GMT +1).

With a knowledge base and work history that spans the globe and more than 20 years, Dr. Dehlinger-Kremer understands the nuances of variations in regulatory standards around the world. She will help you anticipate the regulatory issues you must address in multi-country studies and will identify some key differences between EMA and FDA regulations.

Attendees of this webinar will learn:

  • The rationale behind the changes in the previous Clinical Trials Directive
  • Timeline and meeting the preconditions for the new EU clinical trials regulation
  • Core components
  • Country-specific aspects of the regulation
  • Impacts on sponsors
  • Some cautions: Differences between FDA and EMA regulations
  • Advantages of the new EU clinical trials regulation

To learn more about this event visit: The New EU Clinical Trials Regulation: What You Need to Know Before 2016.

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 (from pharmaceutical & biotech companies, private & academic research institutions, healthcare centers, etc.) 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.

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