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Chiesi Global Rare Diseases and Protalix BioTherapeutics Announce European Commission Authorization of PRX-102 (pegunigalsidase alfa) for the Treatment of Fabry Disease

/PRNewswire/ Chiesi Global Rare Diseases, a business unit of the Chiesi Group established to deliver innovative therapies and solutions for people affected.

United statesUnited kingdomHa afonChiesi farmaceuticiChuck padalaDiego ardigDror bashanAlessio pappagalloAdam daleyChiara travaginGiacomo chiesiProtalix biotherapeutics incChiesi groupEuropean medicines agencyPfizer incDrug administration

How To Overcome Headwinds In Securing Funding For Rare Disease Research

The current landscape is challenging to navigate, but the good news is that there are new and emerging business strategies and funding models to.

Giacomo chiesi

Chiesi sponsors provider of US lab spaces for networking potential

Chiesi partners with BioLabs to gain access to certain sites and work with the companies using the facilities to advance rare disease research.

France generalUnited statesBaden wübergAmryt pharmaGiacomo chiesiNovo nordiskBioinnovation labsGolden ticketGolden ticketClinical developmentDrug deliveryContract manufacturing amp logisticsMarkets amp regulationsLinical evolutionPis active pharmaceutical ingredientsDelivery formulations

Chiesi Global Rare Diseases Announces U S Networkwide Sponsorship of BioInnovation Labs

Chiesi Global Rare Diseases Announces U S Networkwide Sponsorship of BioInnovation Labs
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United kingdomBaden wübergFrance generalUnited statesVeena krishnappaAdam daleyGiacomo chiesiChiesi groupB corpBerry company public relationsGlobal rare diseasesBioinnovation labsStrategic innovation unitBenefit corporationChiesi global rareGolden tickets

Chiesi acquires Amryt Pharma to increase combat of rare diseases

International pharmaceutical company, Chiesi, has taken on Amryt Pharma Plc to show its commitment to developing treatments for rare diseases.

United statesGiuseppe accogliAmryt pharmaGiacomo chiesiB corpChiesi groupChiesi global rareGlobal rare diseasesClinical developmentRare diseaseClinical trialsData managementAtient centricity

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