Tracey Duffy is the First Assistant Secretary of the Medical Devices and Product Quality Division in the Therapeutic Goods Administration – which is part of the Department of Health and Aged Care. Her responsibilities include medical device regulation, Good Manufacturing Practice medicine inspections and Laboratory testing.
Tracey has held several leadership roles within the Department of Health, including in Health Technology Assessment. Tracey also has private sector experience including consultant health and aged care advisory roles.
Tracey is the current Chair for the International Medical Device Regulators Forum (IMDRF) Personalized Medical Devices Working Group and was honoured to Chair the IMDRF Management Committee in 2022.