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World Evidence, Pricing and Access Congress

Connect with our teams and global healthcare leaders as we convene in Amsterdam at the World EPA Congress 2024, the largest European congress in market access, pricing and evidence featuring 300 speakers, multiple streams and over 1500 attendees. 

Meet with us at booth #92
JCA

March 12, 2024 at 12:45pm CET 

EU HTA: How to ensure stakeholder alignment on a national level to accelerate broad patient access? 

Don’t miss our panel on the European Health Technology Assessment (HTA) to explore strategies for achieving stakeholder alignment at national level and speeding up patient access. Moderated by Herbert Altmann, Head of Market Access, Pricing and Reimbursement Europe, at Cencora, the panelists will include Neil Grubert, an independent Global Market Access Consultant, Mihai Rotaru, Director Market Access at EFPIA, and Casper Paardekooper, partner at Vintura, part of Cencora.

Meet the Cencora team

Herbert Altmann
Head of Market Access, Pricing and Reimbursement Europe, Cencora
Casper Paardekooper
Partner, Vintura, part of Cencora
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Ruairi O’Donnell
Senior Director, Evidence Generation & Value Communications, Cencora
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David Ringger
Director, Global Market Access Strategy, Cencora

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Our global biopharma consulting capabilities

When launching products in Europe and HTA countries, we provide deep understanding of the environment, competition, and considerations for market access. We evaluate how your product many be viewed by payers and assess what may be needed beyond your clinical trials. We can help you engage early with key decision-makers and provide timely advice on strategy and execution.

Health economics & outcomes research

Work with industry-recognized experts who apply scientific methodologies to conduct the full scope of health economics and outcomes research for effective strategic planning. We combine rigorous, technical expertise with an understanding of local markets and multiple disease states to deliver relevant, transparent, and credible results to help inform practical strategies and tactics that communicate a robust portfolio of value-based evidence.

Market access consulting

When launching products outside the U.S., we provide deep understanding of the environment, competition, and considerations for market access across Europe and HTA countries. We evaluate how your product many be viewed by payers and assess what may be needed beyond your clinical trials. 

Real-world evidence

With strategic global data partnerships in the US, Germany, the UK, the Netherlands, France, Sweden, Canada, Japan, and China, we support our clients' global strategies along the entire product lifecycle.

Our databases are sourced from administrative claims, electronic medical records, or disease registries, and capture patient-level health information and outcomes for healthcare services performed in various care settings.

Regulatory affairs

Our global team offers the full range of regulatory services needed to enter and operate in international markets. Our strong foundation of technical, regulatory, and scientific expertise, makes us uniquely positioned to support pharmaceutical operations worldwide.

Patient Safety (Pharmacovigilance)

Along the whole product lifecycle from discovery through launch, our international team provides true end-to-end solutions for pharmacovigilance system & operation as well as benefit-risk-management services. Our global footprint enables us to cover all needs worldwide, on local affiliate level as well as for the global & headquarter functions.

Quality management and compliance

From innovation to commercialization, our global teams provide strategy consultancy on all things that impact the quality and compliance of the final product.

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