China NMPA Regulations and Processes for Medical Devices

12.0
RAC Credits
Monday, 15 March 2021 (9:00 AM) - Tuesday, 16 March 2021 (5:00 PM) Eastern Time (US & Canada)

China has become the second-largest economy in the world and one of the most important markets for international businesses. As a regulatory professional, it is imperative to have a sufficient understanding of China’s NMPA regulations, processes, and expertise to navigate the NMPA system.

This workshop will focus on the fundamentals of Chinese NMPA regulations for medical device, providing a systematic review of all elements in the Chinese regulations from clinical trial, 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.

Pricing Amounts & Deadlines

18 November 2020 – 15 February 2021:  Early Bird $800 Member | $900 Nonmember

16 February 2021 – 14 March 2021:  Regular $900 Member | $1000 Nonmember

 

Who Should Attend?

This workshop is suitable for RA professionals with more than 3 years of experience, looking to broaden his/her knowledge base on international regulations or to focus on the Chinese market in the near future.

 

Faculty

 Chang-Hong Whitney  RAC MBA

President & CEO, Whitney Consulting Ltd.

Speakers to be added

 

Cancellation Policy

RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.

All cancellation requests must be submitted in writing via our online cancellation form. RAPS is unable to accept cancellations by phone. Please specify the name of the person registered and event title.

Substitutions may be accepted with written approval from RAPS and must be submitted to raps@raps.org. 

 

If you have questions or concerns, please contact RAPS customer service at +1 301 770 2920, ext. 200, or via email at raps@raps.org.