Medical Device Laws and Regulations in Asia – 2 Part Web-Series 2019
04 Apr 2019
Webinar
Description
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
Past Events
Medical Device Laws and Regulations in Asia – 2 Part Web-Series 2019 - 04 Apr 2019, Webinar (82962)
Important
Please, check "Medical Device Laws and Regulations in Asia – 2 Part Web-Series" official website for possible changes, before making any traveling arrangements