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Health Economics & Outcomes Modeling

Evidence-Backed Economic Models for Life Sciences

A therapy's value has to be demonstrated twice: once in the clinic, and once in the economics. Payers, HTA bodies, and formulary committees expect models that quantify that value transparently, with every assumption open to inspection and every input traceable to evidence.

MadeAi combines AI-accelerated evidence synthesis with hands-on health economics expertise to build the models those decisions rest on: cost-effectiveness and cost-utility analyses, budget impact models, Markov and patient-level simulations, and network meta-analyses. Every model is open-cell and audit-ready, built to ISPOR good practice and the methods guidance of the agencies you are submitting to.

Health Economics & Outcomes Modeling

AI-Powered Health Economics

60%

Faster Screening & Extraction

50-60%

Operational Cost Savings

>99%

SME + AI Accuracy

100%

Scalable & Repeatable Success

Explore our ROI White Paper to learn how these results were measured, benchmarked, and validated, with detailed methodology and real-world outcomes.

madeai
services

Build the Economic Case Payers Can't Argue With

Our platform and modeling experts support the core analyses behind pricing, reimbursement, and access decisions, each built to the good practice standards reviewers apply, including:

Deliverables

Tailored Stakeholder Reports

Our team delivers evidence tailored to the specific needs of regulatory, market access, clinical, and scientific stakeholders.

Tailored Stakeholder Reports

Health Technology Assessment & Market Access

Evidence structured for the HTA submissions and payer conversations that decide access.

Clinical & Evidence Strategy

Landscape, comparator, and evidence gap analysis to inform development and positioning decisions.

Scientific Publications & Medical Communications

Peer-reviewed manuscripts, congress materials, and scientific narratives built on synthesized evidence.

Regulatory & Compliance

Submission-ready documentation with every claim linked back to its source.

RIGOUR

Compliance & Good Practices

MadeAi supports model and dossier development aligned with recognized HEOR, evidence synthesis, and market access standards. Economic models follow ISPOR good-practice recommendations, while reporting adheres to CHEERS 2022 standards. Systematic reviews strictly apply PRISMA 2020 principles, and US formulary dossiers align with AMCP Format 4.1/5.0.

We tailor each deliverable to the specific methodological and submission requirements of key health technology assessment (HTA) bodies—including NICE, IQWiG, Canada’s Drug Agency (CDA-AMC), PBAC, and the EU Joint Clinical Assessment (JCA) framework.

Expert Team

Human Expertise, Enhanced by AI

Our team combines therapeutic knowledge, regulatory experience, and AI expertise to deliver high-quality, reliable outputs.

Therapeutic Area Experts

Deep clinical expertise across a wide range of therapeutic areas, including oncology, rare diseases, and immunology.

Regulatory & Market Access

Hands-on submission experience across NICE, EMA, FDA, and global payer bodies.

AI-Skilled Domain Specialists

Subject matter experts skilled in AI workflows, combining human judgment with AI efficiency.

MD, PhD & PharmD Professionals

Credentialed clinicians and pharmacologists ensuring clinical validity and scientific rigor at every stage.

Cross-Functional Collaboration

Integrated expertise across clinical, regulatory, and commercial functions to keep evidence aligned and decision-ready.

See what our modeling services can do for you

Book a demo to see how MadeAi connects evidence synthesis to economic modeling, from the first search to the submitted model. Our experts are ready to scope your next CEA, BIM, or NMA!

Health Economics & Outcomes Modeling

FAQ

MadeAi combines AI-accelerated evidence synthesis with expert health economics support to deliver the core analyses behind pricing, reimbursement, and access decisions: cost-effectiveness and cost-utility analyses, budget impact models, Markov and patient-level simulations, and network meta-analyses. Every model is built on a systematically reviewed, traceable evidence base.

Model inputs – efficacy, utilities, costs, and transition probabilities are identified through systematic review on the MadeAi platform, so every input in the model traces back to a screened, appraised source. Evidence synthesis and modeling operate as one connected workflow rather than separate projects.

HTA reviewers and payers examine model structure, assumptions, and inputs in detail before accepting results. Transparent, documented models with traceable inputs move through review faster and hold up under questioning, protecting both the timeline and the credibility of the submission.

Models are structured to align with the methodological expectations of the submission’s target HTA bodies and processes, including national agency requirements and EU-level joint assessment needs, with comparative evidence prepared to matching standards.

When disease progression, recurrence, or long-term outcomes drive the economics, single-step models understate reality. Markov cohort models capture movement through health states over time, and patient-level simulation is used when population heterogeneity or treatment history materially changes results.

MadeAi identifies the trial network through systematic review, assesses feasibility and network connectivity first, then conducts the network meta-analysis with documented methodology, so comparative effect estimates are defensible and ready to feed economic models and dossiers.

Yes. Budget impact and cost-effectiveness models are built with local adaptation in mind: population, pricing, and market-mix inputs are structured so affiliates can localize for each market or plan without rebuilding the underlying model logic.