The Dutch tradition: Sinterklaas at PSR!

The Dutch tradition: Sinterklaas at PSR!

Who comes around in December? Is it someone you remember? It's not Santa Claus🎅🏻, my dear, on December 5 Sinterklaas is here! His helper, who we know as Piet, it is a funny guy indeed! So come together and have fun, the holiday season has begun! Fijne pakjesavond...

Fundraising for Epidermolysis Bullosa (EB)

On 6 March 2018 PSR hosted a Volleybal event for the so-called “Butterfly Children”. These are children that are affected by the rare genetic skin blistering condition, Epidermolysis Bullosa (EB). The evening started with a generous donation of €1500 from Ergomed to...

Rare Disease Day 2018

Rare Disease Day 2018

        We Care About Rare! For Rare Disease Day 2018 we organize a fundraiser for kids with Epidermolysis Bullosa and their families! https://lnkd.in/eVzCU74 for more info on the fundraiser click here https://lnkd.in/eXXn74m  

A LEADING ORPHAN DRUG COMBINATION

Ergomed and PSR Orphan Experts have joined forces, creating an industry-leading rare disease CRO offering. Ergomed’s global reach and PSR’s specialized focus on orphan drug development will enable the improvement of lives of patients and families impacted by rare...

Wishing You A Successful And A Happy 2018!

Wishing You A Successful And A Happy 2018!

The PSR-team wishes you and the whole Rare Disease Community a prosperous 2018! Together, we’ll keep our focus on Patient Centricity in order to help those who battle disease every day.