Services
Consultation on strategic, regulatory, scientific and safety aspects of clinical development in China
IND, NDA and import license applications
Strategic regulatory advice and drug development plans for the Chinese market
Link with regulatory authorities
Professional preparation of medical reports, summaries, and other product information
Expertise in global regulatory affairs
The flow chart of application and approval procedure for clinical trials in China
(Source: http://eng.sfda.gov.cn/WS03/CL0769/61659.html)
Address: 2F, Building 4, 188, Pingfu Road, Xuhui District, Shanghai 200231, P.R. ChinaTel: (86) 21 3367 2666, 400 820 8668 Fax: (86) 21 3367 6446 Email: Marketing@scrcnet.org