Why attend ECRD as a market access executive


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Why attend ECRD as… An executive responsible for: Business Development, Corporate Affairs, Commercial Development, Global Market Access, European Market Access, Planning & Operations, Pricing & Market Access



Learn what industry can expect from the future of the EU cooperation on HTA



Hear from patients first-hand about their needs and experiences and get insight into how to work more efficiently with patient organisations



Evaluate new pathways for collaboration and partnership at all stages of the development chain



Explore the implications of emerging pricing, reimbursement and access trends together with those responsible for the markets



Understand the difficulties and possible solutions for patient access to orphan medicinal products and rare disease therapies



See the full picture of how different elements are coming together at global, regional and country level to support orphan medicinal products discovery, development and availability



Acquire new ideas / best practices on how to develop improved treatment for patients or how to deliver it more effectively



Dialogue with all of the stakeholders shaping your environment: patients, policy makers, regulators, member state representatives, academia, researchers, clinicians, HTA evaluators, payers and industry colleagues – together in one venue



Enlarge your network and be part of a community that is focused on improving the lives of rare disease patients

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