Medtec China releases conference content

^{Medtec China has released the first round of information regarding its “MDiT Forum and Regulation Summit 2018,” a conference the organisers state is one of the most attractive to visitors.}

This year, the conference's main theme surrounds regulation, quality and technology and its content is focused on the visitors responsible for QA/QC, regulation, quality control, regulatory compliance, R&D, design and programme.

This year, the event will talk about the development prospects of the Chinese medical device industry, and analyse the top three regulations and polices which are medical device review and approval system, medical device registrant system, and clinical trial quality management of medical devices.

Also to be held this year is the leading sales conference “Chinese Regulatory Updates and Compliance”. The conference will look at MDSAP updates and FDA inspection and will provide attendees with practical case studies.

For the Quality track, William M. Sutton (FDA assistant country Director of China) has been invited to introduce issues related to MDSAP, such as the process of MDSAP regulatory implementation, how to integrate MDSAP into the quality system with ISO13485, and some case studies.

To lead the trend of medical technology, two new conferences have been launched: “Perspective of end user Design & New Technology A” and “Next-Gen Design & New Technology B”. Furthermore, other innovative and interesting onsite free conference and activities will also be worth attending.

Medtec China will also feature a new exhibition zone called “Medical regulatory street” to cater to the need of regulatory consultant services. A lecture on regulation will also be held for visitors to attend.

Medtec China 2018 is going to be held 26–28 September in Shanghai.