Semi Annual EU Medical Device Regulatory Affairs Conference

November 13-14, 2019 | Brussels, Belgium

Park Inn by Radisson Brussels Airport

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Special Thanks to Our Sponsors

WHO SHOULD ATTEND

Organizations currently manufacturing medical technologies from a wide range of therapeutic areas will find this conference of tremendous interest, given the wide-ranging reach of new regulatory requirements across Europe. With dozens of years of combined regulatory experience specific to the device industry, presenters will address valuable presentations highlighting both the challenges faced by manufacturers, as well as strategies for overcoming the increasingly strict regulatory environment. Executives with the following functions will find this program of specific interest:

  • VPs, Directors & Managers of Regulatory Affairs
  • International Regulatory Specialists
  • Product Registration
  • Qualified Persons

Aaron VandykeContact:

Aaron Van Dyke, Operations Director, Life Science
Q1 Productions
+1 (312) 840-9086
avandyke@q1productions.com

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