Healixia is the Belgian community of all professionals active along the life cycle of medicines, medical devices, in vitro diagnostics & other health related products. Members are active in research & development (including pre-clinical, early clinical and later phases), medical affairs, safety, regulatory affairs and market access in industry, academia, investigator sites, authorities, regulatory bodies or in consultancy.
Healixia provides education, training and networking opportunities within and across each of the 4 domains it represents.
Healixia events
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11 September '25Medical Devices conference
AffligemRead moreWith speakers from FAMHP, industry and other involved stakeholders.
You can already register!
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16 September '25Healixia workshop on RIP role and RIP legislation
DiegemRead moreDuring this workshop, we will work in small groups, where you can discuss different cases, challenges, bumps in the road, best practices,... with peers. Each group will have a lead who is experienced in the RIP role and RIP legislation.
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24 November '25Introduction to Regulatory Affairs 2025
BrusselsRead moreThe course is addressed to people new to regulatory affairs who want to acquire a comprehensive foundation; to regulatory professionals wishing to update their knowledge, and to all collaborators working in close relationship with regulatory affairs and wishing to understand the role of the department.
We thank our sponsors for their support:
