Vice President of QA/RA (APAC), Baxter International Inc

Victoria has almost 20 years of regulatory affairs experience in both multi- national device and US-based industry associations. She currently served as Director for Quality and Regulatory Affairs for Asia Pacific in Cordis

Director, Office of Manufacturing Quality and Vigilance for Medical Devices

International Coordination Officer

Pharmaceuticals and Medical Devices Agency (PMDA), Japan

President, Gren International Health & Trade Cons. 

Treasury & Board Member, Alliance for Safe Online Pharmacies (ASOP Global)

Former Director, Office of Health and Information Technologies, U.S. Department of Commerce

Member Advisory Board, APEC Harmonization Center

Head Medical Evaluation Section, SFDA

MBBS, MPH, FAMM

Tracey Duffy is the head of the Medical Devices and Product Quality Division in the Therapeutic Goods Administration (TGA) in Australia.

Assistant Director

Digital Health Device Division,

Medical Device Evaluation Department,

National Institute of Food and Drug Safety,

Ministry of Food and Drug Safety Korea

US FDA

Executive Secretary
Inter-American Coalition for Regulatory Convergence, MedTech Sector
Lead Tier 2
Medical Device Regulatory Convergence, COVID-19 Project (MDRC)