Vinciane Pirard | Medical - SAI, Chair of IRDiRC Companies Constituent Committee (CCC)
Sanofi

Vinciane Pirard, Medical - SAI, Chair of IRDiRC Companies Constituent Committee (CCC), Sanofi

Vinciane Pirard, MD Vinciane Pirard is a Medical Doctor trained at UCLouvain in Belgium, with an extensive career in the pharmaceutical industry dedicated to rare diseases since joining Genzyme in 2002. She currently serves as Medical Affairs Rare Diseases – Scientific Advocacy and Insights Lead at Sanofi, where she drives global scientific advocacy efforts and generates critical insights to advance care for patients living with rare conditions. Vinciane also serves as the private lead of the IMI SCreen4cARe consortium and is actively involved in the RealiseD initiative, contributing to innovative approaches in clinical trials for rare diseases. In addition, she chairs the Company Constituent Committee at IRDiRC (the International Rare Diseases Research Consortium), reflecting her ongoing commitment to fostering cross-sector collaboration and innovation in the rare disease community.

Appearances:



Pre-congress workshops @ 14:00

Early Diagnosis – What’s Needed to Make Change Happen?

Moving beyond isolated advocacy to accelerate diagnosis, this workshop will holistically explore how early diagnosis fits within the rare disease ecosystem from development of diagnostic technologies, to care pathways and policy frameworks.  It will be based on a three-part discussion to:

- Move beyond purely technical debates

- Elicit a range of opinions and different practices 

- Align with European policy developments in rare diseases.

Day 1 @ 17:10

Screen4care EU IHI project and genomic newborn screening: mid-term results and future plans

  • Screen4care EU IHI project is a collaborative effort aimed at implementing precision medicine in healthcare.
  • Genomic newborn screening is a key component of this project, focusing on early detection and prevention of genetic disorders in infants.
  • Mid-term results of the project show promising outcomes in terms of early diagnosis and personalized treatment plans for newborns.
  • Future plans include expanding the screening program to reach more newborns and integrating genomic data into routine clinical practice.
last published: 21/Sep/26 09:05 GMT

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