2016 - Webinar on Medical Device Laws and Regulations in Asia: China, Hong Kong, Japan and Korea

In this webinar, the speaker will discuss the updated differences in regulatory frameworks (regulatory requirements and compliance) in Asia, intending to help you understand and accurately interpret applicable laws and regulations governing medical devices in China, Hong Kong, Japan and Korea. This webinar will help you expedite the registration process for your devices in these Asian countries.
Areas Covered in the Session :
Updated medical device laws and regulations in China, Hong Kong, Japan and Korea.
Definitions, Device classification and rules
Regulatory framework for medical devices in China, Hong Kong, Japan and Korea.
Regulatory requirements for medical devices including in vitro diagnostic devices in China, Hong Kong, Japan and Korea.
How to identify and address the regulatory requirements
How to establish and maintain systematic methods to meet the regulatory requirements.
How to streamline the regulatory process.
PASS-IT Recommendations: Best Practices
Interactive Q&A session
Who Will Benefit:
Regulatory Affairs Managers, Directors and VPs
Clinical Affairs Managers, Directors and VPs
Quality Managers, Directors and VPs
Quality Managers, Directors and VPs
Compliance Managers and Directors
Sales and Marketing Managers, Directors, and VPs
Complaint Handling and Risk Management Managers and Directors
Site Managers, Directors, and Consultants
Senior and Executive Management
Compliance Officers and Legal Counsel
Business Development Managers, Directors, and VPs