Do not miss the opportunity to understand how you and your company can benefit from entry into one of the fastest-growing and second-largest healthcare market in the world.

In this collaborative workshop with the Australia China Health Accelerator, we explore practical knowledge and optimal pathways to a successful product registration in China from the perspective of a top Chinese medical regulation expert.

YOU WILL LEARN:

• How Australian health-tech startups develop strategies to get their medical products registered in China’s healthcare market.
• What requirements you need to know to comply with the regulations.
• How the Chinese regulatory system differs from Australia, the US and Europe?

OUR SPEAKER:

Mr Yongheng Chang

Former senior government official of the China Food and Drug Administration; Consultant, Expert Committee for Capacity Building and Continuing Education on Medical Devices Innovation and Application of the National Health Commission China

Mr Chang has over 30 years’ work experience in various Chinese government departments of medical regulation. He held senior positions in different departments including Deputy Counsel of the Department of Medical Devices of China Food and Drug Administration (CFDA) and Deputy Director General of CFDA Center for Food and Drug International Exchange.

Now he is the consultant of the Expert Committee for Capacity Building and Continuing Education on Medical Devices Innovation and Application of the National Health Commission China. Mr Chang also has strong experience in studying medical device regulatory and regulation systems in the US, Europe and other western countries.

He is also the founder of the China International Medical Device Regulatory Forum, the world’s biggest annual medical device regulatory conference.

PROUDLY SUPPORTED BY:

Event Details

Date: Monday 30 November 2020

Time: 12:00am – 1:00pm AEDT

Platform: Zoom

Member Cost: Free (normally $25)

General Admission: $35 General Admission (+GST +Booking Fee)