Our HEOR. Your Results.

Health economics and outcomes research (HEOR) has become a strategic imperative for market access, reimbursement, and commercial success. ADVI combines rigorous evidence generation, advanced analytics, and market access expertise to demonstrate value, differentiate therapies, and equip manufacturers with the evidence stakeholders need to make confident coverage and treatment decisions.

HEOR Capabilities

Outcome research

Build the evidence that proves value.

Strong outcomes research is the foundation of successful market access. ADVI designs evidence generation strategies that demonstrate the clinical, economic, and humanistic value of therapies, giving manufacturers the evidence needed to differentiate products, support reimbursement, and improve patient access.

  • Design and execute outcomes research that addresses payer and stakeholder evidence needs.
  • Generate clinical, economic, and patient-centered evidence to support product differentiation.
  • Develop evidence strategies that strengthen launch readiness and lifecycle planning.

Economic Modeling

Quantify value. Support better decisions.

Economic evidence is essential for demonstrating the value of innovative therapies. ADVI develops rigorous health economic models that help manufacturers communicate cost effectiveness, support pricing and reimbursement discussions, and inform strategic decision making throughout the product lifecycle.

  • Develop cost effectiveness, budget impact, and disease simulation models.
  • Quantify long term clinical and economic value for payers and HTA organizations.
  • Support pricing, reimbursement, and market access strategies with defensible economic evidence.

Health technology assessment (HTA) AND GLOBAL MARKET ACCESS

Navigate global reimbursement with confidence.

Market access depends on meeting increasingly complex evidence requirements around the world. ADVI helps manufacturers develop integrated evidence and pricing strategies that satisfy HTA agencies, demonstrate value, and accelerate reimbursement across global markets.

  • Develop evidence packages that align with HTA and payer expectations.
  • Support global pricing, reimbursement, and market access strategy.
  • Demonstrate clinical effectiveness, cost effectiveness, and real-world value to decision makers.

Value Comminucations

Turn evidence into compelling value stories.

Scientific evidence creates value only when stakeholders understand it. ADVI transforms complex clinical and economic data into persuasive communications that help payers, providers, and healthcare decision makers recognize the value of innovative therapies.

  • Develop AMCP dossiers, global value dossiers, and payer evidence packages.
  • Create scientific publications, presentations, and reimbursement communications.
  • Build compelling value messaging and commercial tools that support product adoption.

Real world evidence

Generate insights that reflect real world care.

Real-world evidence answers critical questions that extend beyond clinical trials. Leveraging advanced analytics, patient-level data, and deep expertise, including ADVI’s CMS VRDC capabilities, we help manufacturers generate evidence that supports reimbursement, market access, and lifecycle strategy.

  • Design and execute real-world evidence studies using claims and other healthcare data.
  • Analyze treatment patterns, clinical outcomes, healthcare utilization, and economic impact.
  • Generate evidence that supports payer engagement, regulatory strategy, publications, and lifecycle management.

ADVI brings senior-grade operator fluency that seamlessly unites policy, HEOR, and market access. They didn’t just give us advice; they left our entire business stronger than when they found us.

Insights

Real analysis from people who’ve been there

RAND/UCLA Modified Delphi Panels

ADVI Health partners with pharmaceutical and biotech organizations to advance their evidence generation and market access strategies. We support complex research questions through primary research (e.g., …

Caitlin Sheetz, MPH
June 23, 2026

Precision Medicine

Test Ordering Simplification Will Not Be Optional in the Near Future: Why Labs Must Act Before May 26, 2028

The Centers for Medicare & Medicaid Services’ (CMS) Administrative Simplification: Adoption of Standards for Health Care Claims Attachments Transactions and …

Stacey Gilbert, MPH, MBA
May 11, 2026

Precision Medicine

The MolDX Technical Assessment: How to Move Your Test from “Not Successful” to Medicare Coverage Success

In the laboratory space, the MolDX Technical Assessment (TA) is often the moment where the gap between “a great test” …

Stacey Gilbert, MPH, MBA
April 9, 2026

Precision Medicine

CRUSH and Genetic and Molecular Laboratories: A Potential Shift in Medicare Oversight

Genetic, molecular, and reference laboratories are closely watching a new Medicare concept known as CRUSH- short for Comprehensive Regulations to …

Stacey Gilbert, MPH, MBA
March 17, 2026

Oncology/biologics Precision Medicine

March Is Colorectal Cancer Awareness Month: Why CMS’s Proposed NCD 210.3 Update Could Accelerate Patient‑Centered Screening Access

Colorectal cancer (CRC) screening saves lives, but only when patients are able to access care in a way that meets …

Stacey Gilbert, MPH, MBA
March 17, 2026

MFN shifts from noise to credible threat

Throughout 2025, MFN-like concepts were diffuse background noise. That volume intensified in Q4, when legislative and regulatory conversations crystallized around …

Marc Samuels, JD, MPH
March 16, 2026

Cell and Gene Precision Medicine State Policy

The 2026 Rare Disease Reality

Orphan drugs now represent approximately 20 percent of total prescription spend, and over 52 percent of the cell and gene …

Marc Samuels, JD, MPH
February 26, 2026

Precision Medicine

A New Era for Cancer Detection Begins with the Sewell MCED Law

We are seeing a long‑anticipated and important policy inflection point.  By now you might have heard that Congress passed the …

Stacey Gilbert, MPH, MBA
February 11, 2026

FAQs

Discover how ADVI helps life sciences and healthcare companies navigate the intersection of reimbursement, health economics, market access, and health policy from pipeline to brand maturity.

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