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6 questions with Kyle Noonan

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Recap AMCP 2024: Our thought leadership in action

Q&A Interview: Navigating the launch of ATMPs in Europe

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Benefit-driven pricing: How AMNOG strikes a balance between the financial burden on statutory health insurance and reimbursement of innovative medications in Germany

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Embarking on the EU HTAR realization journey: Key insights from the first of six implementing acts

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EAMS evidence: A key player in drug value proposition and NICE approval?

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HTAQ Summer 2024

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Market access brochure

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Anticipating issues, tackling challenges: Next steps with the JCA

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Are alternative access pathways the key to success for small pharma in European markets?

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Government Reliance on Value Assessments in Medicare Part B

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Webinar Insights: Navigating the changing landscape of Inflation Reduction Act (IRA) negotiations 

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Navigating new access hurdles in Europe: A conversation with Cencora’s EU HTA Lead

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Is NICE’s disease severity classification at risk?

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HTA Quarterly Spring 2024

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Rating the robots: Artificial intelligence for literature reviews

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It’s Just…So…Cool – Don’t miss your opportunity for JSC!

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Apples to apples, or apples to oranges? Comparing the Inflation Reduction Act to drug-pricing programs in other countries

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Executive Insights: What's next with the Inflation Reduction Act (IRA)

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Planning for the World: Q&A With Sandra Anderson, SVP of International Commercialization at Cencora

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Addressing Barriers to Patient Care for People Living With Atopic Dermatitis

Shaping the future of healthcare: Our thought leadership at ISPOR Europe 2023

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Anticipating the top seven global market access trends for 2024: Cencora’s healthcare landscape outlook 

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Podcast: How 2023 will shape the US Biosimilar space for 2024 and beyond

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The Dutch Lock Procedure for Reimbursement: Ensuring Effective and Affordable Healthcare

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Enhancing Patient-Reported Outcomes (PROs) in German AMNOG Assessments: Insights from the ISPOR Europe 2023 Conference

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Will the IRA hinder the potential of Biosimilars?

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Patients at the center – Does the JCA truly embrace the patients’ voice?

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Exploring the Implications of Differing PICO Criteria for Oncology Drug Assessments in Europe

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Unlocking the Potential of Joint Clinical Assessment (JCA) in Europe: Insights from Industry Leaders and Experts

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Webinar on demand: Implications of the EU JCA on patient access and engagement

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Cost and resource burden of coverage with evidence development

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Does the EU HTAR really put patients at the center?

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HTA Quarterly Winter 2023

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Navigating the way to the new EU JCA—Are biopharma companies, HTA bodies, patients, and clinicians sufficiently prepared? 

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Gauge the impact: What does the striking down of a federal copay accumulator regulation mean for patients and copay programs?

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Valuing potential cures: An examination of ICER’s approach to assessing high-impact single and short-term therapies

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First 10 drugs for Medicare price negotiation announced under IRA

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Q&A – Preparing for the EU Joint Clinical Assessment (JCA) process

HTA Quarterly | Fall 2023

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Only 17 months until the implementation of the new EU JCA—Latest developments and remaining uncertainties

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The cures conundrum: The importance of getting value assessment right for transformational therapies

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VPAS—Where next?

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Podcast: Collaborative perseverance to bring change to medicine access

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Multistakeholder perspectives on Joint Clinical Assessment in Europe

Panel explores insights and implications of the game-changing EU JCA

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Pharma Europe Q&A

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Empower your people and brand with biopharma learning solutions

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On-demand webinar: The EU JCA process: Opportunities and challenges in bringing innovative medicines to patients in Europe

Reimbursement considerations for home infusions

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How the JCA may help to address medicine inequality across Europe

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Recap Asembia 2023: Our impactful contributions to the premier specialty pharmacy conference

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Recap AMCP 2023: Our thought leadership in action

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Answering four key questions about HTA market archetypes

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Six essential steps for emerging biopharma companies launching a new therapy

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New pan-EU HTA: How can biopharma navigate the joint clinical assessment?

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Innovation spotlight: Adding nursing support to at-home clinical trials