Wednesday, October 27th 2021 (09:00) - Thursday, November 18th 2021 (18:30)


Brussels, Belgium


€1649.99 for non-members



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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. 

Programme description:

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.

Programme agenda:

  • 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


  1. Dr. Hugues Bogaerts

  2. Prof. Pieter Neels

  3. 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.