4th Annual EU Medical Device & Diagnostic Quality Management Workshop
December 4-5, 2019 | Frankfurt, GermanyLe Meridien Frankfurt Hotel
NOTIFIED BODY SPEAKERS:
Marta Carnielli
IVD Technical Officer
TÜV SÜD
Michael Bothe
Co-Head of Certification Body Active Medical Devices
DQS MEDIZINPRODUKTE
Sabine Ohse
Head of Notified Body IVD
MDC – MEDICAL DEVICE CERTIFICATION
MEDICAL DEVICE & DIAGNOSTIC INDUSTRY SPEAKERS:
Matthias Bürger
VP Global Regulatory & Quality Assurance
ZIMMER BIOMET
Stefanie Leschonsky
VP Quality & Regulatory Affairs
DRÄGERWERK
María José López
Manager Quality Compliance CCV
EDWARDS LIFESCIENCES
David Lansbergen
Manager Regulatory Affairs & Quality, EMEA
SAKURA FINETEK EUROPE
Ulf Grundmann
Partner
KING & SPALDING LLP
Erik Vollebregt
Partner
AXON LAWYERS
Melissa Finocchio
Sr. Director, Global Quality – Business & Support
BIOMERIEUX
Angeles Sanfrancisco
Manager International Quality Compliance
EDWARDS LIFESCIENCES
Wolfgang Werner
Senior VP Regulatory & Quality
BIOVOTION
Isabelle Kohlstetter
QRA Manager Integration, Distribution & SQA EMEA and QRA Lead Northern Europe
CARDINAL HEALTH
Noel Butterworth
EU PDO, Quality & Operations Manager
MEDTRONIC
Carsten Krafcsik
Head Regulatory Affairs Switzerland
TECAN
Peter Linders
Director Global Regulations & Standards
PHILIPS HEALTHCARE
Mayda López-Belmonte
Director Quality & Regulatory Compliance Spain, and Innovation EMEA
JOHNSON & JOHNSON
Martin Geertsema
EMEA Director, Quality Assurance & Regulatory Affairs
CONMED
Yana Pozhidaeva
Associate Director, Clinical Quality Assurance
ABBOTT
Yana Pozhidaeva
Associate Director, Clinical Quality Assurance
ABBOTT