Semi Annual EU Medical Device Regulatory Affairs Conference

November 13-14, 2019 | Brussels, Belgium

Park Inn by Radisson Brussels Airport

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DISTINGUISHED PRESENTERS INCLUDE:

REGULATORY AUTHORITY & NOTIFIED BODY SPEAKERS:

Valérie Nys
MDR Program Manager
FEDERAL AGENCY FOR MEDICINES & HEALTH PRODUCTS, BELGIUM

Bassil Akra
VP Global Strategic Business Development
TÜV SÜD Product Service

Michael Bothe
Co-Head of Certification Body, Active Medical Devices
DQS MEDIZINPRODUKTE

Dr Matthias Neumann
Deputy Head, Medical Devices Safety Unit
BMG, GERMAN FEDERAL MINISTRY OF HEALTH

Bart Mersseman
Global Medical Devices Certification Manager, Head of NB
SGS BELGIUM

MEDICAL DEVICE INDUSTRY EXPERTS:

Rita Peeters
Sr Director Regulatory Affairs Policy & Intelligence EMEA
JOHNSON & JOHNSON

Frank Matzek
VP Regulatory & Governmental Affairs
BIOTRONIK

Momchil Blagoev
Director Corporate Regulatory Affairs
EDWARDS LIFE SCIENCES

Kemine Hale
Senior Manager Regulatory & Clinical Affairs
ADVANCED BIONICS

Fayez Abou Hamad
MD Vigilance Expert
TERUMO EUROPE

Vladimir Murovec
Associate, Life Sciences
SIMMONS & SIMMONS

Mary Gray
Associate Director EU MDR UDI
JOHNSON & JOHNSON

Erik Raadsheer
Sr Director Governmental, Regulatory Affairs & Quality Assurance EMEA
ALIGN TECHNOLOGY

Michel Marboeuf
Senior Director Corporate Regulatory Affairs
STRYKER

Koen Cobbaert
Chair Software Focus Group
COCIR
Senior Manager Quality, Standards & Regulations
PHILIPS

Annabelle Bruyndonckx
Counsel
SIMMONS & SIMMONS

Hendrik Heinze
Director Quality & Regulatory
BERLIN HEART

Carine Cochereau
VP International Regulatory Affairs
INTEGRA LIFESCIENCE
Chair Clinical Investigation Taskforce
MEDTECH EUROPE

Andrea Sparti
Regulatory Affairs Manager
CENDRES+MÉTAUX

Elizabeth Gfoeller
Corporate Director, Regulatory Affairs
MED EL

Juliette Cook
Regional Regulatory Director EMEA
COCHLEAR

Jens Pfannkuche
Director Regulatory Affairs
PENUMBRA EUROPE

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