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Tuesday, February 5 • 16:00 - 17:30
#DMD5: The Convergence of Medicines, Medical Devices and Analytics

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Component Type: Session

Is the new European legislation on medical devices sufficient enough to handle the new paradigm of convergence between advanced medicinal products / diagnostics / apps / algorithms et al? Are we ready as regulators?


Thomas Senderovitz, DrMed, MD


Setting the Scene
Thomas Senderovitz, DrMed, MD

Panel discussion
Elena Bonfiglioli

Panel discussion
Karl Broich, DrMed

Panel discussion
Lindsay Edwards

Panel discussion
Jorgen Scholler


Elena Bonfiglioli

Managing Director, Health and Life Sciences, Microsoft
avatar for Karl Broich

Karl Broich

President, Federal Institute for Drugs and Medical Devices (BfArM), Germany
Physician, MD (certifications in Neurology, Psychiatry, Behavioural Psychotherapy). BfArM in Bonn (Germany): 2000 to 2014 several executive functions, since 08/2014 head (President). Work in several EMA committees. Current research: clinical trials methodology CNS, biomarkers in drug... Read More →

Jorgen Scholler

Head of Division. Department of Health Technology, Techincal University Denmark
avatar for Thomas Senderovitz

Thomas Senderovitz

Chair of HMA Management Group; Director General, Danish Medicines Agency
Thomas Senderovitz took over as Director General of the Danish Medicines Agency on 1 April 2016. His career includes more than 20 years working with medicinal products and he has held several senior positions in international biopharmaceutical Companies. He previously worked at the... Read More →

Tuesday February 5, 2019 16:00 - 17:30 CET
Hall D Austria Center Vienna Bruno-Kreisky-Platz 1 1220 Vienna Austria
  DIAmond Sessions, Session
  • Featured Topics Regulatory Science
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