Getting on Hong Kong's voluntary list now will lead to product registration in the near future. Like many other Asian countries, Hong Kong is developing a more regulated, harmonized system for medical device manufacturers and importers. Though registration is currently voluntary, manufacturers will soon be required to register their products. Get a head start by attending our webcast and familiarize yourself with Hong Kong's medical device regulations. The speakers is Pacific Bridge Medical's executive in our Hong Kong office. Real case studies will be used to emphasize key points. This 90-minute session will include a 60-minute presentation, followed by 30 minutes of Q&A.

What you will learn:

- Overview of Hong Kong Healthcare

- Hong Kong Medical devices Market Industry

- Overview of Hong Kong medical device regulation

- Hong Kong Regulatory Bodies

- Medical Device Classification

- Medical Device Administrative Control System

- Medical Device Application

- Labeling requirements

- CAB (Conformity Assessment Bodies)

- Local Responsible Person (LRP)

- Post-marketing surveillance and quality control

- Reimbursement

- Adverse Event Reporting

- Case Study

- Hong Kong Business Culture

For more information visit http://www.researchandmarkets.com/research/z2tjbp/hong_kong_medical