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
