7TH ANNUAL EU DEVICE AND DIAGNOSTIC REGULATION CONFERENCE

SEPTEMBER 25-26, 2017 | BRUSSELS, BELGIUM | PARK INN BY RADISSON BRUSSELS AIRPORT
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DISTINGUISHED PRESENTERS INCLUDE:

COMPETENT AUTHORITY & NOTIFIED BODY SPEAKERS:

Hugues Malonne
Director General, DG “Post-Authorization”
FAMHP – FEDERAL AGENCY FOR MEDICINES & HEALTH PRODUCTS, BELGIUM

Prodromos A. Kaplanis
Head of Medical Devices Authority
CYMDA, MINISTRY OF HEALTH – CYPRUS

Bassil Akra
VP – Global Focus Teams, Cardiovascular, Orthopedic & Clinical
TÜV SÜD PRODUCT SERVICE GMBH – GERMANY

Sue Spencer
Global Service Line Director – Regulatory
UL

MEDICAL DEVICE & IVD INDUSTRY SPEAKERS:

Matthias Bürger
VP of Quality Assurance & Regulatory Affairs EMEA
ZIMMER BIOMET

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

Peter Schrutka-Rechtenstamm
Senior Director, Global Regulatory and Clinical Affairs
CARL ZEISS MEDITEC

Susana de Azevedo Wäsch
Head of Global Regulatory Affairs
GEISTLICH PHARMA

Luminita Tulea
Senior Manager Regulatory Affairs EMEA
BECKMAN COULTER

Claudia Solimeo Meneghisse
Senior Regulatory Affairs Manager
TECAN

Marianna Hofer Orfanidou
Head RA Implant Systems Early Markets

NOBEL BIOCARE

Céline Bourguignon
Director Global Regulatory Policy, WW Gov. Affairs & Policy
JOHNSON & JOHNSON

Rainer Voelksen
VP Quality & Regulatory Affairs
OCCLUTECH

Lukáš Bican Prikryl
Quality & Regulatory Manager CEE, EEDC
BECKMAN COULTER

Elizabeth Gfoeller
Corporate Director, Regulatory Affairs
MED-EL

Leo Hovestadt
International Regulatory Affairs & Quality Assurance Director
ELEKTA

Yves Ohandja
Manager Quality & Regulatory Affairs Europe
IMMUCOR

Matthias Binder
Senior Regulatory Affairs Manager
CROMA PHARMA

Philippe Auclair
Senior Director of Regulatory Strategy & Advocacy
ABBOTT LABORATORIES

Mayda Lopez-Belmonte
Director Business Quality South, UK/Ireland and POLO EMEA
JOHNSON & JOHNSON

Carsten Krafcsik
Head Regulatory Affairs Switzerland
TECAN

Arkan Zwick
Corporate Director Regulatory Affairs
CROMA PHARMA

David Lansbergen
Regulatory Affairs & Quality Manager, EMEAI
SAKURA FINETEK EUROPE

Carole Robin
Director Regulatory Affairs, Clinical & Quality
3-D MATRIX EUROPE

Elena Kyriacou
Director & Founder
ELEMED

Steve Ellison
VP of EU Sales
PRISYM ID

LEGAL SPEAKERS:

Jana Grieb
Counsel
MCDERMOTT WILL & EMERY

Annabelle Bruyndonckx
Of Counsel
SIMMONS & SIMMONS

Emmanuel Garnier
Managing Associate
SIMMONS & SIMMONS

Karina Hellbert
Attorney-at-Law & Head of Life Sciences
FIEBINGER POLAK & PARTNER RECHTSANWÄLTE