|
As Asia’s third largest market for medical devices, Korea’s regulations are changing rapidly to accommodate the growing influx of medical products. Registering your product and getting reimbursed can be very difficult in Korea; therefore, understanding the regulatory issues is key in being successful in this growing market. This webcast will focus on the existing and new Korean medical device regulations. This 90-minute session will include a 60-minute presentation, followed by 30 minutes of Q&A.
PLEASE NOTE THAT THIS WEBCAST, UNLIKE OUR OTHER WEBCASTS, WILL NOT BE AVAILABLE FOR SALE AFTERWARDS.
What you will learn:
- Country Overview
- Medical Device Market
- KFDA
- Pre-market Requirements
- Pre-market Process
- Product License
- Business License
- KGMP
- Post-marketing Surveillance
- Adverse Events
- Reimbursement
- Recent Changes in Regulations
Each dial-in number is $400.00.
This webcast will take place on April 23, 2008 and will start at 11:00 AM US Eastern Daylight Savings Time.
|
Print
This Page 