The medical device regulatory reform in China is changing the pattern and future of the enterprises and the whole industry at an unprecedented pace.
What benefits will the enterprises gain from the reform? How should the enterprises understand and make use of these regulatory advantages?
The RAMED Regulatory Forum, with its team of experts having years of regulatory experience and coming from world famous medical device firms, will share the up to date CNDA requirements with you.
Forum topics:
1. Organizational development for MD administration in China/Chang Yongheng;
2. To be a winner by regulatory solution for innovative MD in China /Ellen Jiang;
3. CNDA Requirement update for MD Pre-market approval /Christine Jiang;
4. CNDA Acceptance for overseas clinical data/ Christine Jiang & Ellen Jiang;
5. China Medical Device Market Characteristics /Jane Shen;
Time: Jul 26, 2018, 11:30am-2:00pm
Location: Charles Room, 14th floor CIC, One Broadway, Kendall Square, Cambridge, MA 02142, USA
Registration Link: http://events.constantcontact.com/register/event?llr=8jjeod6ab&oeidk=a07efhwmix2dbceddb6
Professional Strengths of Presenters:
Yongheng Chang, Executive Chairman of the China International Medical Device Regulatory Forum (CIMDR) of the CCFDIE of CNDA.
He was Director of Product Registration Division of the Department of Medical Devices of SFDA (State Food and Drug Administration)
Ellen Jiang, 22 Years RA & Compliance leader experiences in China for medical devices
Christine JIANG, 12years+ RAQA experience in MNC
Jane Shen, 20 years+ hands on and leadership experience in China and other Asian markets in medical devices filed.