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...

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...
Antareslaan 41
2132 JE Hoofddorp
The Netherlands
Tel: +31 23 303 69 00
Fax: +31 23 303 69 99
Email: info@psr-group.com
Send