24 - 25 October, 2017 | Munich, Germany

Meet the Speakers

Speakers


Margaret  Kelly
Margaret Kelly
Device Development Project Leader
Novartis
Heidi  Manijeh Mehrzad
Heidi Manijeh Mehrzad
Principal Consultant
HFUX Research
Helene  Gustafsson
Helene Gustafsson
Head of Regulatory & Clinical Compliance
Leo-Pharma
Peter  Czuczman
Peter Czuczman
Senior Manager, Technical and Global Project Leader
BTG
 Lori-Ann  Woodard
Lori-Ann Woodard
Sr Manager Quality Compliance Combination Products
Teva
Andrew Love
Andrew Love
Vice President
Be4ward Ltd
Steve Dew
Steve Dew
Associate Director Combination Products and Medical Devices
Biogen
René   Dathe
René Dathe
Head of Quality Medical Devices Shared Function
Novartis
Jussi  Haikarainen
Jussi Haikarainen
Sr Development Manager, Pharmaceutical Sciences Platform
Orion
Drew  Rogers
Drew Rogers
Global Director for Healthcare & Medical
Trelleborg Sealing Solutions
Sofia  Ribeiro
Sofia Ribeiro
Head of Quality for Projects and Technology Transfers
Bayer
Stefania  Ragone
Stefania Ragone
Pharmaceutical Assessor Licensing Division
MHRA
Lars  Hyveled-Nielsen
Lars Hyveled-Nielsen
Regulatory Project Director Regulatory Affairs & Safety
Zealand Pharma
Edwin  Schumacher
Edwin Schumacher
Managing Partner
Synergio
Audrey  Clarembeaux
Audrey Clarembeaux
Manager Head of Medical Device Development QA
UCB
Florian  Tolkmitt
Florian Tolkmitt
Independent Regulatory Affairs and Clinical Evaluation Expert
Keith  Summerhayes
Keith Summerhayes
Managing Director
MDCRQ Solutions Ltd
Thomas  Brzoska
Thomas Brzoska
Clinical Evaluation and Regulatory Affairs Expert