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Plenary
Sabina Hoekstra-van den Bosch, PharmD, FRAPS
Regulatory Strategy Principal
TUV SUD Product Service GmbH
Ede, Gelderland, Netherlands
Gert Willem Bos, FRAPS
CTO, Executive Director & Partner at Qserve Group
Qserve Group (Netherlands)
Baarn, Utrecht, Netherlands
Simon Richards, PhD
Vice President Divisional Regulatory Affairs
Abbott Rapid Diagnostics
Scarborough, Maine, United States
Natascha J. Cuper, PhD
Clinical expert
DARE Medical Certifications
Woerden, Utrecht, Netherlands
Erica Conway, PhD
Global Head - In Vitro Diagnostic Medical Devices
BSI (London)
Milton Keynes, United Kingdom
Waldo Weijers, PharmD
Senior Advisor
Medicines Evaluation Board (NL)
Utrecht, Utrecht, Netherlands
Eric Klasen, MSc
RA & Quality consultant in Life Sciences
Founder of Waypoint Consulting
Féchy, Switzerland
Armin Ritzhaupt, PhD, MPH
Scientific Administrator
European Medicines Agency
Micha Nuebling, PhD
Head Department
Paul-Ehrlich-Institut
Langen, Hessen, Germany
Jayanth K. Katta, PhD
Senior Regulatory Lead
BSI
Milton Keynes, England, United Kingdom
Bassil Akra, PhD
CEO
QUNIQUE GmbH
Greifenberg, Bayern, Germany
Elizabeth Gfoeller, MA
Corporate Director, Regulatory Affairs
Med-El
Innsbruck, Tirol, Austria
Erik Raadsheer, PhD
Sr. Director, Regulatory & Government Affairs and Quality Assurance, EMEA
Align Technology, BV.
Susana Waesch
Biotechnologist and vice president
Ypsomed
Klaus-Dieter Ziel
Managing Director
MEDCERT GmbH, Notified Body Germany
Hamburg, Germany
Erik Hansson
Deputy Head of Unit Medical Devices and Health Technology Assessment
DG for Health and Food Safety (SANTE)
Brussles, Brussels Hoofdstedelijk Gewest, Belgium