International Niemann–Pick Disease Alliance

The Global Community supports INPDA’s letter to EMA

The International Niemann-Pick Disease Alliance (INPDA) has organised a letter (see below) voicing the perspective and concerns of the NPC community, which will be sent to the European Medicines Agency (EMA) next week. Families also have the opportunity to support by adding their signature using this link: https://forms.gle/oZw91YVTn3ivWU348

 

INPDA Letter to CHMP March 2022

Join the Registry

Calling all patients and carers! We've created a global registry of all NPD patients - if you're not enrolled yet, join us now...

The Impact of NPC

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