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ISPOR EU 2024: Expert strategies to transform evidence and value-based outcomes

September 30, 2024

The biopharmaceutical, diagnostic, and device industries are experiencing a period of great change. Policies are evolving, payer environments are shifting, the concept of value is expanding, and great science is no guarantee of frictionless, in-market patient access. 

Our expert team will be at ISPOR EU 2024 in Barcelona, Booth #1412. Our specialists in global and US policy, access, value, and evidence are eager to discuss ways to advance and accomplish your strategic goals. 

 

Meet the global and US specialists at Booth #1412

Advance your research and outcomes strategies by tapping into our expert network at ISPOR EU 2024.

Contact us and schedule your meeting

 

As challenges and the definitions of value continue to evolve, it’s crucial to adapt your access strategies accordingly. From payer to point of care, Avalere Health is ready to guide you through these complexities with our first-class capabilities in HEOR, market access, value engagement, and policy.

Tim Wright

President, Global Policy, Access, Value, and Evidence

avatar for Tim Wright - President, Global Policy, Access, Value, and Evidence

 

Gain insights from our 34 research posters accepted for ISPOR.

We are proud to have 34 research posters accepted for ISPOR EU 2024. View our research at Booth #1412 or contact us for a deeper discussion, tailored to your specific needs. Our research posters at ISPOR EU 2024 span a broad range of insights, including: 

 

  Increasing collaboration between stakeholders — navigating the impact of policy changes
  • Recent trends from UK’s cancer drugs fund, key drivers of acceptance HTA197
  • Comparison of ‘coverage with evidence development’ approaches for digital health technologies and pharmaceuticals MT31
  • Contrasting evidence requirements for early access schemes for DHTs in the UK and Germany: a challenge for multi-market evidence generation planning MT16
  • The devil in the detail: the challenges of evaluating patient access to medicines HPR107
  • Analysis of pharmaceutical company actions in Asia-Pacific to improve patient access OP6
  • Real-world evidence in action: a review of Australia’s health technology assessment (HTA) of non-drug health technologies MT2
  • Evolving national HTA frameworks in the Asia-Pacific region: a targeted literature & stakeholder review of HTA processes in Australia, Japan, and South Korea HTA72
  • Next-generation sequencing-based circulating tumor DNA testing: clinical drivers versus market access reality MT69
  • Insights on early access refusal in France HTA28

 

  Capturing and demonstrating holistic value and patient impact under increasing evidence
  demands
  • Determining if Delphi panel qualitative insights can be useful when informing drug pricing-related decisions in the drug development stage SA18
  • Addressing postnatal depression: disparities in treatment availability HSD59
  • Postnatal depression: an underestimated humanistic burden in maternal health PCR86
  • How does real-world evidence support regulatory and HTA agency assessments and beyond? RWD183
  • NICE quality-adjusted life years severity modifier: what have we learned so far HTA282
  • Is there enough focus on capturing health-related quality of life perspectives of pediatric patients and their caregivers in non-oncology indications? PCR81
  • Exploring the impact of changes in health valuation post-COVID-19 pandemic on existing cost-effectiveness analyses EE485
  • How has treatment switching been accounted for? Insights from NICE appraisals HTA106
  • Defining value in the mental illness space: how are patient preferences accounted for in health technology assessments of treatments for depression and schizophrenia? HTA45
  • Integrating healthcare system value into new innovations for timely and full patient access HPR160

 

Our Avalere Health expertise in health outcomes and novel approaches to leveraging data into insights is on full display at this year’s ISPOR EU. With a record number of acceptances, our collective team has demonstrated the value of our work across a broad and complex set of research questions.

Laura Housman

Senior Vice President, US Evidence & Strategy

avatar for Laura Housman - Senior Vice President, US Evidence & Strategy

Join us for our panel discussion: Refining value assessment by considering indirect costs

Date and time: Tuesday, November 19, 11:45 AM
Panel: 219
Theme: Discover the benefits of broadening the scope of value assessment by incorporating evidence on the indirect burden of disease. We’ll explore its application in US value assessment and ex-US Health Technology Assessment (HTA) submissions.

Key discussion points
  • Rare diseases often require a significant amount of medical care, which leads to a higher burden of direct medical costs.
  • Indirect costs—such as productivity loss, absenteeism, lifestyle disruptions, and family and societal impacts—contribute to the overall burden of patients with rare disease and their caregivers.
  • These broad indirect impacts are often overlooked and under-measured, leading to underestimation of the total disease burden in evidence used for value assessments and HTA submissions.
What you’ll learn
  • Recent research measuring the indirect burden of disease
  • How real-world evidence on indirect costs can be applied to value assessment and HTA submissions
  • The potential impact of incorporating these insights on healthcare decision making

 

Value assessment is most accurate when we consider costs and benefits in a holistic way. Explore real-world examples of measuring indirect burden in our discussion at ISPOR EU 2024.

Jan McKendrick

Executive Director, Global HEOR

avatar for Jan McKendrick - Executive Director, Global HEOR

 

Schedule your meeting at ISPOR EU 2024

Take advantage of our deep knowledge across global and US markets, providing a unique insight into investment decisions, clinical development programs, and product lifecycle planning.

Schedule a meeting

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