UNDERSTANDING CFDA’S NEW REGULATIONS ON DEVICE MANUFACTURING

About the Product
Includes 1 hour and 25 minute Windows Media Video File and PowerPoint presentations for immediate download.

John Balzano from Covington and Burling speaks on developments in the regulation of medical device manufacturing in China over the last two years. In 2014, China overhauled its entire medical device regulatory system. That reform is related to a number of new measures to increase supervision of medical device manufacturers in China and raise the quality of domestically produced devices. This presentation includes an overview of the reformed manufacturing license system, new good manufacturing practices, contract manufacturing issues, and inspections and enforcement issues, as well as a perspective on potential future reforms.

Speaker:
John C. Balzano
Of Counsel
Covington & Burling LLP

Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:

• Regulatory Affairs
• Legal
• Quality Assurance

Contact:

Brooke Akins | Division Director, Life Science Programs
+1 (312) 224-1693 | bakins@q1productions.com​