Medical Device Laws and Regulations in Asia Part 1 China 2019 is a webinar that covers topics such as:
- Definitions, Device classification and rules
- Updated medical device laws and regulations in China
- Regulatory requirements for medical devices including in vitro diagnostic devices in China
- Regulatory framework for medical devices in China
- 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
Medical Device Laws and Regulations in Asia Part 1 China 2019 is intended for:
- 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
