UDIs and Traceability for Medical Devices 2018

Key topics for this year’s forum include:
- Ensure your company is 100% ready for upcoming regulations with case studieson the impact of changes to European and US regulatory changes and global UDI frameworks
-Streamline your labelling verification processes and maintain regulatory compliance with targeted presentations that examine compliance requirements
-Protect your products and enhance your anti-counterfeiting strategy through access to international customs and product data with the World Customs Organisation’s IPM program case study
-Outline your data strategy and ensure that you maximise the utilisastion of your product data to safeguard product supply with Masimo and MedTech’s industry leading advice
and much more...