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Meet the Program Commitee for 2025!
项目委员会
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Stuart Finnie, DrSc, MS • Senior Director, CMC RA Policy and Advocacy
Gilead Sciences, United Kingdom -
Sabina Hoekstra-van den Bosch, PharmD, MSc, RPh • Global Director Regulatory Strategy
Tüv Süd, Netherlands -
Antonella Cardone • Director
Cancer Patients Europe, Belgium -
Aimad Torqui • Head of Division European cooperation and veterinary affairs
MEB, Netherlands -
Dimitrios Athanasiou, MBA • Patient Advocate
WORLD DUCHENNE ORGANIZATION (WDO) , MDA HELLAS, Greece -
Claudia Dollins, PhD, RAC • Vice President, Precision Medicines, Global Regulatory Affairs
GlaxoSmithKline, United States -
Estelle Michael • Policy and public affairs lead
UCB, Belgium -
Gracy G Crane, PhD, MS • Policy Lead
Roche, United Kingdom -
Inka Heikkinen, MBA, MSc • Regulatory Policy Lead
Lundbeck, Denmark -
James Whitehead, MBA, MSc • Former Senior Director Device & Digital Safety - AstraZeneca
Visiting Lecturer - Pharmacovigilance MSc Course, University of Hertfordshire, United Kingdom -
Kate Porch • Associate Director, Global Labeling Centre of Excellence
Johnson & Johnson, United Kingdom -
Lada Leyens, PhD, MSc • Senior Director, EUCAN regulatory head GI
Takeda, Switzerland -
Magda Chlebus, MA • Executive Director, Science Policy & Regulatory Affairs
EFPIA - European Federation of Pharmaceutical Industries and Associations, Belgium -
Mark Pellett, PhD, MSc, RPh • Senior Director and Group Manager
AstraZeneca, United Kingdom -
Momir Radulovic • Executive Director
Slovenian Medicines and Medical Devices Agency (JAZMP), Slovenia -
Monique Al, PhD • Special advisor CCMO
Central Committee on Research Involving Human Subjects (CCMO), Netherlands -
Nikos Dedes • Representative
European AIDS Treatment Group (EATG), Greece -
Rebecca Lumsden, PhD • Head of Regulatory Science & Policy EU/AMEE
Sanofi, United Kingdom -
Sabine Haubenreisser, PhD, MSc • Principal Scientific Administrator, Stakeholders and Communication Division
European Medicines Agency, Netherlands -
Sarah Pope Miksinski, PhD • Executive Director, CMC Regulatory Affairs
Gilead Sciences, United States -
Susanne Ausborn, PhD • Global Head International Regulatory Policy
Roche, Switzerland -
Tamara Di Carlantonio, MA • Regulatory Policy Lead
Roche, Switzerland -
Thomas Møller, MBA, MSc • Senior Director Global Regulatory Affairs - Devices
Novo Nordisk, Denmark -
Tim Powell • Director, Submission Sciences, Global Safety and Regulatory Sciences
Biogen, United Kingdom -
Ursula Busse, PhD, MBA • CMC Regulatory Affairs Advisor
Self Employed, Switzerland -
Willemijn van der Spuij, MSc • Executive Director Europe | International - Patient Safety
Bristol Myers Squibb, Switzerland