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The World Orphan Drug Congress Europe returns 27-29 October 2025 as the largest and most established orphan drug & rare disease meeting of its kind!
 
From cell and gene therapy, genetic testing, and market access, to real world evidence, this one meeting covers the whole orphan drugs value chain where science, government and manufacturers all come together to create groundbreaking progress.
 
Limited FREE passes are available for Sanofi employees in France and Netherlands, granting full access to the conference, including the workshop day, networking app and drink receptions.
 
Please note: all applications are subject to Terrapinn approval and availability. We also have the right to decline or withdraw your application at any time.
 
 

 

Sanofi will be contributing sessions across the entire programme  – see who will be speaking below:
 
 

28 October

 


 11:30

Alicia Granados
Global Health Scientific Advocacy & Insights Medical Affairs, Rare Diseases
 
Working Group
Involving Rare Diseases Patients in Clinical Guidelines’ 
Development 
 
 

29 October

 
 

 

12:15

Alicia Granados
Global Health Scientific Advocacy & Insights Medical Affairs, Rare Diseases
 
Access & Pricing
How do you assess evidence in Rare? The work of HTAi RDIG

 

 
 

 
 15:00

Anne-Sophie Chalandon
Head of Rare Diseases Global Public Affairs Rare Disease and ATMP Policy at Sanofi, and leading the IFPMA Rare Diseases Group
 
 
Keynote Panel: In what way can we mobilise, enable and leverage international policies around the world for PLWRDs?

 

 
 
 
Offer applies to Sanofi employees only. All guest pass applications subject to Terrapinn approval.

Get involved at World Orphan Drug Congress Europe 2025

 

 

TO SPONSOR


Steph Scanlon

Steph.Scanlon@terrapinn.com

 

TO SPEAK


Abdu Kauroo
Abdu.Kauroo@terrapinn.com

 

MARKETING & PRESS


Jasper Cameron

Jasper.Cameron@terrapinn.com

 

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