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Session 4: Medical Devices and Technology
Session Chair(s)
Yasha Huang
Head of Regulatory Policy Asia Pacific, Global Regulatory Policy & Intelligence
Roche Diagnostics, Singapore
With the rapid advancement in medical technology and digital solutions, are the current regulatory mechanism still fit for purpose? What are the regulatory agility elements that we have observed from the COVID-19 journey could potentially accelerate patient access to innovative technologies? Please also join our prestigious panelists to take a closer look at the real world evidence and how could it be leveraged in clinical evaluation to support innovation and improve patient access.
Speaker(s)
Roundtable: Fit-For-Purpose Regulations for Software / Digital Solutions
Roberta Sarno
APAC Med, Singapore
Head Digital Health Committee
Contributing Round Table Speaker
Varun Veigas
Roche Diagnostics Asia Pacific Pte. Ltd, Singapore
Leader- Policy and Strategic Partnerships, Health Policy and Patient Access,
Contributing Round Table Speaker
John Richard Thornback
Diagnostics Development Hub, Singapore
Chief Operating Officer,
Contributing Round Table Speaker
Manan Hathi
Styker, United States
Senior Manager, Regulatory Affairs
Regulatory Agility / Reliance in the Background of COVID-1
Rama Sethuraman
Health Sciences Authority, Singapore
Director, Medical Devices
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