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Meet the Program Commitee for 2022!
项目委员会
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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 • Head of International Regulatory Policy and Innovation

Takeda, 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

Bristol Myers Squibb, Belgium -
Ronnie Mundair • Regional Labelling Head - Canada and LATAM - Senior Director

Pfizer, United Kingdom -
Rodrigo Palacios, MBA • Senior Director, Technical Regulatory Policy

F. Hoffmann-La Roche Ltd., 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 Senior 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