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Illuminate your path to market by leveraging real world data and insights to substantiate your value story and facilitate stakeholder decision-making

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Effectively articulate your scientific breakthrough to enable healthcare providers, regulators, payers, and patients to understand the value of your product

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Lumanity is about transformation; we apply incisive thinking and decisive action to cut through complex situations and deliver transformative outcomes to accelerate and optimize access to medical advances Our Story
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Innovation doesn’t guarantee success. But when diverse minds come together to focus on key issues, incredible change can unfold. Lumanity embraces unique viewpoints and experiences to develop better solutions and improved outcomes for patients.
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Patient Engagement

Inflation Reduction Act

Cell and Gene Therapy

Biotech

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Perspectives
View Expert Perspectives on the Use of Generative AI in Medical Publications

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Latest Lumanity and AVEO Oncology Win MediaPost Planning & Buying Award for Best Use of Data

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We are Changemakers. Whether you’re an experienced professional or a recent graduate, join Lumanity to make a difference. We are a collaborative, global team—no matter where you live, you can help us build a healthier world.

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London SE1 1PP
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Perspectives

The IRP Regulatory Pathway and its Implications for NICE

In this report, we summarize NICE's advice on using the IRP when seeking earlier marketing authorization from the manufacturer's perspective.

View Dec 3, 2024

Transform Your Competitive Strategy

View Dec 2, 2024

Are EU Member States Ready?

View Dec 2, 2024

Navigating Real World Evidence Requirements

Whitepaper Dec 2, 2024

ISPOR Europe Diaries 2024

View Nov 29, 2024

Real World Evidence Expertise in Duchenne’s and Beckers Muscular Dystrophy

The PHARMO Institute, part of Lumanity, delivers research insights into Duchenne's muscular dystrophy (DMD) and Beckers muscular dystrophy (BeMD), and the PHARMO Data Network offers great research potential for these rare disease populations.

Resource

Using Real World Data to Guide Precision Oncology Drug Development

View Nov 25, 2024

Biopharma Commercialization Readiness: What Leaders Need to Consider

Resource

Upgrading ADCs to the Next Level: What Does the Future of Antibody Drug Conjugates Look Like?

On-Demand Webinar Nov 20, 2024

Searching in a More Complete Haystack: Using Real World Data to Guide Precision Oncology Drug Development

On-Demand Webinar Nov 13, 2024

The IRA Impact on Innovation in Drug Development

IRA Impacts on Innovation in Drug Development Insights from patient advocacy groups regarding the IRA’s impact on treatment advancements Shifts in drug development priorities within biotech firms and their discussions with investors Projected effects of the IRA on innovation, particularly for specific patient populations

On-Demand Webinar Nov 13, 2024

How to: Conduct an HTA Landscaping Review

Resource

Payer Value Communications: Advancing Effective Value Messages in an Evolving Access Landscape

On-Demand Webinar Nov 8, 2024

Case Study Scenario: IRA Threatens Advancement in Fight Against Rare Cancers

View Nov 7, 2024

Healthcare’s Bold New Reality: Key Insights from HLTH 2024

View Nov 5, 2024

Regional Considerations and Challenges in Integrated Evidence Generation Planning (IEGP)

Podcast Nov 5, 2024

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