Economic modelling
Markov, partitioned-survival, decision-tree, and microsimulation models — built in Excel/VBA or R, with clear technical documentation and model walkthroughs.
Health Economics & Management Consulting · Hong Kong
Zephyr VitaLink International partners with biopharmaceutical, medical device, payer, and public-health clients to translate clinical and real-world data into defensible economic value — across access, reimbursement, and policy.
Services
We design and execute the analytical work that supports reimbursement, formulary, and policy decisions — combining health economics rigour with the practical needs of commercial, medical, and government affairs teams.
Cost-effectiveness, cost-utility, and cost-minimisation analyses built on transparent Markov, partitioned-survival, or decision-tree models — calibrated to local payer perspectives and clinical pathways.
Payer-ready budget impact models that quantify the financial implications of introducing a new technology across populations, settings, and time horizons — with scenario testing for uptake, mix, and pricing.
End-to-end support for health technology assessment submissions — evidence synthesis, value dossiers, response strategies, and stakeholder engagement aligned to local HTA frameworks across APAC and beyond.
RWE generation plans that anticipate evidentiary gaps before they appear — from study design and data source selection to analysis, publication, and integration into ongoing value narratives.
Independent evaluation of public-health programs and reimbursement policies — quantifying clinical, economic, and equity impact for ministries, payers, hospitals, and not-for-profits.
Clear, credible, audience-tuned value stories — for payers, clinicians, policymakers, and internal stakeholders — supported by visualisations, objection handling, and field-ready materials.
Methods & Approach
Every engagement is anchored to internationally recognised standards — ISPOR Good Practices, CHEERS, PRISMA, and local HTA guidance — with documented assumptions, reproducible code, and structured uncertainty analysis.
Markov, partitioned-survival, decision-tree, and microsimulation models — built in Excel/VBA or R, with clear technical documentation and model walkthroughs.
Systematic literature reviews, indirect treatment comparisons, and network meta-analyses — feeding directly into economic and value evidence packages.
Parametric survival modelling, flexible spline approaches, and external-data calibration — with structured plausibility assessment of long-term extrapolations.
Cohort, case-control, target-trial emulation, and propensity-score approaches across claims, EMR, registry, and primary-collection data.
Deterministic and probabilistic sensitivity analyses, value-of-information frameworks, and scenario stress-testing — communicated for decision-makers, not just modellers.
Distributional cost-effectiveness analysis and equity-informed appraisal — surfacing trade-offs that aggregate ICERs can hide.
Sectors & Stakeholders
Our work sits at the intersection of clinical evidence, economic value, and policy — serving the organisations that fund, deliver, and regulate care.
Global, regional, and emerging companies preparing for launch, reimbursement, or lifecycle management decisions.
Manufacturers building economic and clinical value cases for novel devices, diagnostics, and digital health tools.
Public and private payers seeking independent evaluation of coverage decisions, formulary design, and benefit packages.
Ministries of health, HTA bodies, and public agencies designing or evaluating reimbursement and public-health programs.
Health systems and provider networks evaluating service-line economics, technology adoption, and program design.
Not-for-profits, foundations, and global-health organisations evaluating interventions across LMIC and APAC contexts.
Consulting Process
We start by understanding the decision the work needs to support — payer, regulator, policymaker, or internal — and agree on the question, evidence base, and success criteria.
We map the evidence landscape, identify gaps, and design the analytical approach — model structure, data sources, comparators, and reporting outputs.
Models, analyses, and dossiers are built against documented standards, with peer review, validation against published benchmarks, and structured uncertainty analysis.
We translate results into stakeholder-ready outputs — dossiers, decks, interactive tools — and support clients through HTA review, payer engagement, and policy dialogue.
As evidence and policy evolve, we update models and narratives — keeping the value story aligned with the latest data, comparators, and decision-maker priorities.
Why Zephyr VitaLink
You work directly with the people who design and build the analyses — not a delegated junior team. Less translation loss, faster iteration, better evidence.
Every model and analysis is built to withstand HTA review, peer critique, and internal audit — aligned with ISPOR, CHEERS, and local technical guidance.
We understand local payer structures, HTA pathways, and clinical practice patterns across Greater China and APAC — and connect them to global value strategies.
Deliverables in English and Chinese, structured for global teams and local stakeholders — without compromising on methodological clarity.
Documented assumptions, traceable data, and reproducible code. Clients can defend the work long after the engagement closes.
We disclose interests, decline conflicts, and structure engagements so that analytical integrity is never in question — especially in evaluative work.
About the Firm
Zephyr VitaLink International Limited is a Hong Kong–incorporated health management consultancy. We were founded to bring senior, methodologically rigorous health economics support to clients across Asia-Pacific — particularly those navigating fragmented payer landscapes, evolving HTA frameworks, and accelerating real-world evidence requirements.
Our practice combines formal training in health economics, epidemiology, and public health with hands-on experience supporting reimbursement, policy, and program evaluation across both established and emerging markets.
Contact
Share a few details and we will respond within two business days to scope a short discovery conversation. All enquiries are treated as confidential.
Hong Kong SAR
By appointment