Introduction to European Regulatory Affairs 2014 is a conference dedicated to current EU regulatory requirements and procedures including:
- Integrate CTD requirements
- Speed-up the MAA
- Compile and present the key information
- Gain faster response from the regulators
- Improving dossier compilation process
- License maintenance
- Taking into consideration the patent situation
- Facilitating drug’s successful review
Introduction to European Regulatory Affairs 2014 brings together:
- Those moving into regulatory affairs from other areas within a pharmaceutical company
- Regulatory Affairs professionals seeking to improve their skills in the regulatory environment
- Regulatory Affairs, Registration and Documentation assistants/officers/managers
- Anyone wishing to update their knowledge on European regulatory affairs