Description: This workshop will focus on the fundamentals of Chinese NMPA regulations for medical devices, providing a systematic review of all elements in the Chinese regulations from clinical trials, to quality management, product registration and post-market surveillance. Led by instructors who are veteran regulatory managers, this workshop will also incorporate personal experience, knowledge, up-to-date information and best practices.

Location: Online

Organiser: RAPS

Contact: +1 301 770 2920, ext. 200