EU Medical Device Post-Market Clinical Evaluation Planning Conference

Caroline Dore Geraghty
Director of Medical Devices & Head of the Notified Body
NATIONAL STANDARDS AUTHORITY OF IRELAND

Robert Madjno
Director, Clinical Assessment
TÜV SÜD

Pedro Eerdmans
Head of the Notified Body
DEKRA CERTIFICATION BV

Klaas Van’t Klooster
Clinical Manager
JOHNSON & JOHNSON

Andreas Gmerek
Senior Manager Medical Scientific Affairs
B. BRAUN AVITUM AG

Yanela González
Principal Clinical Research Manager
NOBEL BIOCARE

Michal Slomczykowski
Medical Director
GEISTLICH PHARMA AG

Elizabeth Weathers
Clinical Research Manager
IBA GROUP

Lincoln Tsang
Partner
ARNOLD & PORTER

Karsten Wallbrück
Director Regulatory & Clinical Affairs Europe
ABIOMED EUROPE GMBH

Barry Sands
President & Founder
RQMIS, INC.

Paola Vivoda
Head of Clinical Operations, EMEA
ZIMMER BIOMET

Ruben Roijers
Manager, Q&R – Post-Market Surveillance
PHILIPS HEALTHCARE

Benedikt Þorri Sigurjónsson
Manager of Clinical Evaluation, Medical Office
ÖSSUR

Sabine Konopka
Director Clinical Affairs
PHENOX GMBH ELIZABETH WEATHERS

Josefine Sommer
Senior Associate
SIDLEY AUSTIN LLP

Rita Herrenknecht
Clinical Program Manager Cardiac Surgery
LIVANOVA

Jón I. Bergsteinsson
Co-Founder and VP of Global BD
SMART-TRIAL

Simon Crowe
Senior Business Development Manager, Medical Device Partnerships
CASTOR EDC