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What to expect at Medtec China

More than 900 professional delegates and 60 speakers are anticipated at this year’s Medtec China, which will be held from 14th to 16th September in the Shanghai World Expo Exhibition and Convention Center.

Attendees

The “MDiT Forum and Regulation Summit” plans to bring local and international experts from the medtech field, as well as technical principals of medical device companies. Keynote speakers from NIFDC, Tianjin Medical Devices Supervision and Testing Center CFDA, CCCMHPIE, SHFDA’s Division of Medical Device Registration, JSDA, GDMDT, FDA China and Shenzhen Mindray Bio-Medical Electronics, have been invited to attend.

Conference

This year's "Chinese Regulatory Updates and Compliance" will interpret the latest updates of regulatory hotspots, including the Covid-19 pandemic. The event will also deliver insight from experts about the future of the medical device industry.

Quality Track A will still focus on "Management of Medical Product Life Cycle” and analyse the risk and quality management of medical device products over the entire life cycle from the perspective of manufacturers.

Quality Track B will discuss "FDA's Shift from 21 CFR 820 Toward ISO 13485: 2016 and FDA factory inspection" and analyse the changes that will result from the FDA's change in quality regulatory system and its impact on factory inspections.

The technology track will launch eight conferences including:

Additionally, this year there will be three new technology forums titled:

Conference sponsorship opportunities are available, and currently nearly ten conferences have been pre-booked to meet the most appropriate customers face-to-face.

The event anticipates attendance from more than 500 exhibitors and 250,000 professional visitors to negotiate business, purchase and exchange technologies.

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