Do you want to understand the activities and specific requirements for the clinical development of a vaccine?
This training session highlights the highly demanding activities and specific requirements of regulatory characteristics – the quality, safety, efficacy, and also clinical trial performance in the development of vaccines.
This course gives you the answers to the differences with pharmaceutical trials, identifies the challenges, and lets you understand the biological business. We have updated the programme this year, to include a practical workshop on assessing risk/benefit ratio from the point of view of the regulator and the manufacturer.
27 October - 09:00 to 12:00
08 November - 17:00 to 18:30
09 November - 17:00 to 18:30
15 November - 14:00 to 15:00
16 November - 14:00 to 16:00
18 November - 14:00 to 16:00
Dr. Hugues Bogaerts
Prof. Pieter Neels
Prof. Pierre Van Damme
Who should attend?
Managers & scientists involved in clinical research with vaccines
Regulatory managers of biological medicinal products
Project Managers & Clinical Research Associates (CRAs) working with biological medicinal products
Professionals in these fields wishing to refresh their knowledge and skills
Click here to register.