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Meet the Program Commitee for 2022!
Program Committee
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Petra Doerr, PharmD, RPh • Director
European Directorate for the Quality of Medicines and Healthcare (EDQM), France -
Sini Eskola, MPharm, MS, MSc • Director Regulatory Strategy
EFPIA - European Federation of Pharmaceutical Industries and Associations, Belgium -
Marco Greco, PhD • President
European Patients' Forum, Belgium -
Sabine Haubenreisser, PhD, MSc • Principal Scientific Administrator, Stakeholders and Communication Division
European Medicines Agency, Netherlands -
Niklas Hedberg, MPharm • HTACG Co-Chair & Chief Pharmacist
Dental and Pharmaceutical Benefits Agency, TLV, Sweden -
Volker Liebenberg • Chief Medical Officer
Elypta, Sweden -
Alan Morrison, PhD • Vice President Regulatory Affairs Intl
MSD, United Kingdom -
Karen A Noonan, MA • Senior Vice President, Global Regulatory Policy
Association of Clinical Research Organizations (ACRO), United States -
Sibilia Quilici • Executive Director
Vaccines Europe, Belgium -
Tim Buchanan • Senior Director, Clinical Lead, Tau, Neurology Patient Value Unit
UCB Biopharma, Belgium -
Manuel Haas, PharmD, MSc • Executive Director - Regulatory Affairs Europe
MSD UK, United Kingdom -
Rebecca Stanbrook, RPh • EFPIA ICH E6(R3) Expert Working Group Member
Switzerland -
Matt Popkin, PhD • Senior Director, CMC Excellence, Global Regulatory Affairs
GSK, United Kingdom -
Diane Wilkinson, PhD, RPh • Executive Director, Global CMC Regulatory Affairs
AstraZeneca, United Kingdom -
Thomas Brookland, MSc • Regulatory Science and Policy Lead
F. Hoffmann-La Roche Ltd, Switzerland -
Douglas Gregory • Senior Director, Government Affairs Strategy and Excellence
Bristol Myers Squibb, Belgium -
Ronnie Harprit Mundair • Regional Labelling Head - AfME, Canada and LATAM - Senior Director
Pfizer, United Kingdom -
Rodrigo Palacios, MBA • Senior Director, Technical Regulatory Policy
F. Hoffmann-La Roche, Switzerland -
Henrik K. Nielsen, PhD, MBA, MSc • Vice President
Novo Nordisk A/S, Denmark -
Isabelle Stoeckert, PharmD, PMP • Independent Regulatory Science Expert
Independent, Germany -
Álmath Spooner, PhD • Head of Europe Regulatory Policy & Intelligence (RPI)
Abbvie, Ireland -
Raphael Van Eemeren • EU QPPV Director, Global Patient Safety
Amgen AB, Sweden -
Alison Cave, PhD • Chief Safety Officer
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom -
Patrice Verpillat, DrMed, MD, PhD, MPH • Head of Real World Evidence
European Medicines Agency, Netherlands -
Rick Vreman • Patient Access Manager
Roche, Netherlands -
Nadege Le Roux, PhD • Regulatory Policy Senior Director
Bristol Myers Squibb, Switzerland -
Andras Incze • Founder & CEO, Akceso Advisors AG, Switzerland
University Lecturer Healthcare Management, B-W State University, Germany, Switzerland -
Piers Mahon • Senior Principal and European Leader
Oncology Evidence Networks, IQVIA, United Kingdom -
Bettina Ryll • Member of the First EU Cancer Mission Board
MPNE, Vision Zero Cancer, Sweden