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

        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  

Wishing You A Successful And A Happy 2018!

Wishing You A Successful And A Happy 2018!

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...

Disorder: the Rare Disease Film Festival. October 3rd, Boston USA.

Disorder: the Rare Disease Film Festival. October 3rd, Boston USA.

Acquisition of PSR Group BV, a specialist orphan drug CRO, for consideration of up to €5.7 million  and  Placing to raise £2.9 million Acquisition moves Ergomed towards leadership in orphan drug development services PSR's specialist orphan drug development business...

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Email: info@psr-group.com
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