Health Economics & Outcomes Modeling
Evidence-Backed Economic Models for Life SciencesA 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.
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.
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:
Reimbursement conversations eventually arrive at one question: is the added benefit worth the added cost? Cost-effectiveness and cost-utility analyses answer it in the units HTA bodies work with, cost per QALY and per life-year gained, and reviewers will take the model apart line by line before they accept the answer.
MadeAi builds CEA and CUA models designed for exactly that scrutiny: transparent structure, documented assumptions, and every efficacy, utility, and cost input traceable to a systematically reviewed source. Full sensitivity and scenario analyses show decision-makers not just the result, but how much they can trust it.
Cost-effectiveness analysis is commonly used for:
- HTA submissions and reimbursement dossiers
- Pricing and value-based negotiation support
- Cost per QALY and life-year gained estimates
- Uncertainty and scenario analysis for decision confidence
Before a payer asks whether a therapy is cost-effective, they ask a more immediate question: what happens to our budget if we cover it? A credible budget impact model answers in the payer’s own terms, their population, their horizon, their cost structure.
MadeAi delivers budget impact models that are transparent enough to defend and flexible enough to localize: uptake and market-mix scenarios payers recognize, inputs drawn from a traceable evidence base, and a structure affiliates can adapt to each market without breaking the logic. The conversation starts with credibility instead of caveats.
Budget impact models are commonly used for:
- Formulary and coverage decision support
- Affordability planning across payer populations
- Country and plan-level model adaptations
- Uptake and market-share scenario testing
Chronic and progressive diseases don’t resolve in a single step, and neither should the models that represent them. Markov transition-state models and patient-level simulations capture how patients move through health states over time, so long-term costs and outcomes reflect the true course of disease rather than a snapshot.
MadeAi designs and builds these models with clinical and health economics experts working together: health-state structures grounded in the natural history literature, transition probabilities sourced from systematic review, and patient-level simulation where population heterogeneity or treatment history genuinely changes the answer. Structure first, spreadsheet second.
Markov and patient-level models are commonly used for:
- Modeling chronic and progressive disease pathways
- Long-term cost and outcome extrapolation
- Survival modeling beyond trial follow-up
- Capturing patient heterogeneity in economic results
The comparator that matters to a payer is rarely the one in your trial. When head-to-head data doesn’t exist, network meta-analysis and indirect treatment comparisons provide the comparative effect estimates that HTA submissions and economic models depend on, and assessors expect the methodology to hold up.
MadeAi grounds every NMA in a systematically identified trial network, assesses feasibility before committing, and documents heterogeneity, model choice, and fit to the standards HTA reviewers apply. The comparative estimates flow straight into your CEA and value dossier, one connected evidence chain from search to submission.
Network meta-analysis is commonly used for:
- Comparative effectiveness without head-to-head trials
- Effect estimates for economic model inputs
- HTA and JCA comparative evidence requirements
- Feasibility and network connectivity assessment
Tailored Stakeholder Reports
Our team delivers evidence tailored to the specific needs of regulatory, market access, clinical, and scientific stakeholders.
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.
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.
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.
Choose the Right Engagement Model
Do-It-Yourself
Software as a Service
Done-For-You
Hybrid: Software + SME
Build-Operate-Transfer
Customized Version
Choose which option or combination of support models works best for your business.
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!
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.