Medical Device Laws and Regulations in Asia – 2 Part Web-Series

Medical Device Laws and Regulations in Asia – 2 Part Web-Series is a webinar that covers topics such as:

  • 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

Medical Device Laws and Regulations in Asia – 2 Part Web-Series 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

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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