The Seminar of Medical Device Regulation and Registration in China

In recent years, China has successively amended access policies and regulations of the medical devices since 2014. Along with implementing Regulations for the Supervision and Administration of Medical Devices and related measurements, how oversea enterprises should respond to the regulation change, and how to obtain the CFDA certificate with low cost and high efficiency, it is the big challenge for South Korean companies.
CIRS and Techcode Seoul collaboration have scheduled a meeting “The Chinese Medical Devices Regulations and Registration seminar” in March 18, 2017, Seoul, South Korea to help South Korean companies to understand the new medical devices regulations and how to apply CFDA medical device certificate, to adjust the strategy of China market.
CIRS will build the technology and communication service platform for you, looking forward to your participation.

Meeting Arrangement
Time ： Local time 14:00 - 16:30, March 18, 2017 (Saturday)
Place： 8F, Kait Tower, No.306 Teheran-ro, Gangnam-gu, Seoul,Korea
Language： Korean & Chinese
Meeting agendas

Time March 18, 2017	Content	Guest speaker
14:00-14:10	Techcode Seoul Introduction	Techcode
14:10-14:40	Introduction to Medical Device Management Policy. China's medical device regulation system The status of medical device industry in China The trend of the medical device supervision in China. How the South Korean enterprises to enter Chinese market	Amily Xu Vice president CIRS-CIRSBEIJING
14:40-14:50	Tea Break
14:50-15:50	Overseas medical devices CFDA registration and operation suggestion - China medical equipment update latest regulations - Medical device registration process and data requirements - Overseas medical devices CFDA registration operation Suggestions	Cindy Fu Project Manager CIRS-CIRSBEIJING
15:50-16:30	Q&A or Free discussion

Registration form
Fill in the application form（The attachment）Sent to the email zxj@cirs-group.com

The Organizer：
Techcode
Techcode has established incubation systems in Beijing, Shanghai, Shenzhen, Gu'an, Silicon Valley, Seoul, Tel Aviv, and Berlin to provide innovators with a global entrepreneurial network and the integration of global innovation resources aimed at providing comprehensive service for entrepreneurs. It improves the possibility of entrepreneurship success and accelerates business growth rate. Techcode and CFLD collaboratively open up innovation incubator and industrial value chain by sustainedly incubating high growth entrepreneurial business and being combined with CFLD town mode to realize coordination innovation for sustainable development. http://www.techcode.com/
CIRS
CIRS is a professional product regulatory compliance and technicalconsulting service firm. With its headquarters based in Hangzhou of China and offices and laboratories located in Europe、 Beijing, Nanjing、 Ningbo and Hong Kong.

The CIRS Medical Device Business Unit has a long-term commitment to researching product technology, laws and regulations and industry police of domestic and oversea medical devices. With its professional and technical experiences、 multiple resources and global network, CIRS assist domestic and oversea medical device enterprises with a comprehensive service chain and one-stop solution in medical devices regulation and technical consulting service, including medical devices registration and approval、 clinical trials、 quality management system、manufacturing and distributing license、 technology consulting、 laws and regulations training. We are dedicated to medical devices enterprises gaining competitive advantage by reducing business risks associations with regulatory affairs and removing barrier to entry.。 www.cirs-md.com/md

Contact Us：
禚新杰 (Korean & Chinese)
Email: zxj@cirs-group.com
TEL：+86-571-89716576

會議報名回執|Registration Form

姓 名 Registrants	單 位 Company Name	職 務 Position	手 機 Tel & Mobile	郵箱 Email

Note: Please fill the registration form and send it back to Mr Zhuo: zxj@cirs-group.com