Medical Device Laws and Regulations in Asia - Part 2 - India, Japan, and Korea 2019

Medical Device Laws and Regulations in Asia - Part 2 - India, Japan, and Korea 2019 is a webinar dedicated to medical device laws and regulations in India, Japan, and Korea.

Topics

• Definitions, Device classification and rules
• Updated medical device laws and regulations in India, Japan and Korea
• Regulatory requirements for medical devices including in vitro diagnostic devices in India, Japan and Korea
• Regulatory framework for medical devices in India, Japan and Korea
• How to establish and maintain systematic methods to meet the regulatory requirements
• How to identify and address the regulatory requirements
• PASS-IT Recommendations: Best Practices
• How to streamline the regulatory process
• Interactive Q&A session

Who should Attend

• Clinical Affairs Managers, Directors and VPs
• Regulatory Affairs Managers, Directors and VPs
• Quality Managers, Directors and VPs
• Quality Managers, Directors and VPs
• Sales and Marketing Managers, Directors, and VPs
• Compliance Managers and Directors
• Site Managers, Directors, and Consultants
• Complaint Handling and Risk Management Managers and Directors
• Compliance Officers and Legal Counsel
• Senior and Executive Management
• Business Development Managers, Directors, and VPs