Andrzej Ryś

Principal Scientific Adviser, Directorate-General for Health and Food Safety, European Commission

Commissioner Stella Kyriakides

Commissioner for Health and Food Safety, European Commission

Ali Al-Dalaan

Executive Vice President for Medical Devices Sector, Saudi Food and Drug Administration

Nada Alkhayat

Policy Officer, Directorate General for Health and Food Safety, European Commission

Philippe Auclair

Senior Director, Regulatory Strategy and Advocacy, Abbott Quality and Regulatory

Mariela Aranda

Head of the Service of In Vitro Diagnostic Products, National Institute of Medical Devices

Pat Baird

Head of Global Software Standards, Philips

Elodie Baumfeld Andre

Head of Real World Data, Data & Analytics, Roche

Augusto Bencke Geyer

Head of Medical Devices Office, Brazilian Health Regulatory Agency

David Boudreau

Director General, Health Canada’s Medical Devices Directorate

Gyuhan Chae

Director of Medical Devices Policy Division, Medical Devices Safety Bureau, MFDS

Heather M. Colvin

Director, Evidence & Outcomes Policy, Johnson & Johnson MedTech

Erin Cutts

senior international policy analyst, U.S. Food and Drug Administration

Christophe Driesmans

Head of the Materiovigilance Entity, Federal Agency for Medicines and Health Products

Tracey Duffy

Medical Devices and Product Quality Division, Therapeutic Goods Administration, Australia

Lesley-Anne Farmer

Expert Advisor, Therapeutic Goods Administration

Melissa Finocchio

SVP – Chief Regulatory Officer, SOPHiA GENETICS

Adrien Guenego

Interventional neuroradiologist, Erasme center

Andrea Hanson

Market Analysis Lead, Health Products Regulatory Authority

David Hau

Senior Medical Adviser, Medical Devices Authorisation Branch, Therapeutic Goods Administration

Sabina Hoekstra

Global Director Regulatory Strategy, TÜV SÜD Medical Health Services

Patrick Hope

Chair, DITTA and Executive Director, Medical Imaging & Technology Alliance (MITA)

Leo Hovestadt

DITTA, CIE WG Chair

Xu Jinghe

Deputy Commissioner, National Medical Products Administration (NMPA), GHWP Chair

Hae Ung Lee

Director, Corelinesoft

You-kyoung Lee 

Professor, Laboratory Medicine, Soon Chun Hyang University Hospital

Alexandre Lemgruber

Regional Advisor on Health Technologies Management, Pan American Health Organization

Thomas Linders

Communications professional

Carolina Magnatti

Medical Products Evaluator, National Institute of Medical Products (ANMAT)

Kees Maquelin

Regulatory Affairs Manager, Abbott BV

Tom Melvin

Associate Professor of Medical Device Regulatory Affairs, Trinity College Dublin

Tomoyuki Miyasaka

Deputy Director, Medical Devices Evaluation Division, Pharmaceutical Safety and Environmental Health Bureau, Ministry of Health, Labour and Welfare (MHLW), Japan

Matthias Neumann

Deputy Head Medical Devices Safety Unit, German Federal Ministry of Health

Rolf Oberlin Hansen

International Representative, Danish Medicines Agency

Donal B. O'Connor

Clinical Manager for Medical Devices, Health Products Regulatory Authority

Bryan So

Executive Secretary General , Global Harmonization Working Party

Janet Trunzo

Chair, Global Medical Technology Alliance

Yuan Peng

Division Director, Department of Medical Device Registration, NMPA

Paul Piscoi

Administrator, DG Santé, European Commission

Irena Prat

Team Lead, In vitro diagnostics Assessment, World Health Organization

Jesús Rueda Rodríguez

Director General Strategies, Special Projects and International Affairs, MedTech Europe

Anindita Saha

Assistant Director for the Digital Health Center of Excellence, U.S. Food and Drug Administration

Rama Sethuraman

Director, Medical Devices, Medical Devices Cluster, Health Products Regulation Group, Health Sciences Authority

Bryan So

Executive Secretary General , Global Harmonization Working Party

Nicole Taylor Smith

Global Head of Regulatory Science and Policy, Philips

Miang Tanakasemsub

Regional Regulatory Affairs head, Asia Pacific, Johnson & Johnson

Harriet Teare

Deputy Director of Partnerships, UK Medicines and Healthcare products Regulatory Agency (MHRA)

Melissa Torres

Associate Director for International Affairs, Center for Devices and Radiological Health, U.S. Food and Drug Administration

Paulyne Wairimu

Chair, African Medical Devices Forum (AMDF)

Timothy Wilton

Medical Director, the National Joint Registry

Cheng-Ning Wu

Senior Technical Specialist, Division of Medical Devices and Cosmetics, Taiwan Food and Drug Administration

Daniel Yoon

Acting Manager, International Programs, Health Canada

Lyu Yunfeng

Head of clinical and biostatistics division II, Center for Medical Device Evaluation of NMPA