Medical Device and IVD Regulations in Asia Pacific 2014

Key Topics

• Type testing
• Successful market authorisation and renewal
• Essential advice from SGS Japan and practical insight
• Valuable insight on streamlining external audits
• IVD registration requirements and expectations in Asia Pacific
• Clinical trial and data requirements in Asia-Pacific
• Compliance in post market operations
• Readiness for regulatory change in Asia Pacific

Who should Attend

Heads, Directors, managers, Senior managers and associates of:

• International Regulatory affairs
• Regulatory affairs
• Quality systems
• Global regulatory affairs
• Regulatory compliance
• Quality assurance
• Product registration
• RA/QA