Are European incentives speeding access in rare cancer treatments?
Examining the impact of support programmes for orphan treatments.
Articles/ Pharma Market Access/ UK & Europe/ Views and analysis
Marco Ricci
ema, Europe, orphan drugs, pharma, rare disease, regulation
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Examining the impact of support programmes for orphan treatments.
Articles/ Healthcare/ Views and analysis
Linda Banks
patients, Paul Klee, rare disease, scleroderma
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Highlighting the symptoms of scleroderma, latest research and a genuine ‘diary’ experience from a US patient.
Articles/ Clinical/ Pharma Market Access/ R&D/ Views and analysis
Andrew McConaghie
Alexion, rare disease, Soliris, ultra-rare disease
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Claire
Highly Specialised Technology, orphan disease, patients, rare disease
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Articles/ Audio/ Debates/ Debates/ Debates & Insight/ Debates & Insight/ Market Access/ Patients/ Pharma Market Access/ Webinars/ Webinars On demand
Paul Tunnah
budget, cancer, CF Trust, debate, drug, England, fund, IMS Health, insight, market access, NHS, orphan, Qualie, rare disease, Shire, Tunnah, UK
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