Introduction to European Regulatory Affairs 2014

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

Who should Attend

• 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