HEOR & market access intelligence

Carry evidence from development into value demonstration.

StromaOS connects evidence generation planning, health economics, outcomes research, real-world evidence, value dossiers, payer questions, HTA response, local adaptation, and market learning in one governed execution environment.

Connected value evidence Governed economic models Controlled local adaptation Traceable payer response
The market access operating problem

Evidence is generated by function, but value must be demonstrated as one argument.

Market access and HEOR teams must combine clinical, epidemiological, economic, real-world, patient, utilization, and competitive evidence across markets. That work is frequently initiated late, adapted repeatedly, and managed through disconnected models, documents, vendors, and local processes.

01 · Late evidence alignment

Value questions surface after development choices are fixed.

Payer, HTA, comparator, endpoint, population, outcomes, and economic evidence needs are often discovered after the relevant studies and analyses have already been designed.

02 · Model fragmentation

Economic and outcomes models lose their operating context.

Inputs, assumptions, scenarios, utility values, resource use, comparators, validation, review, and market adaptations are spread across files and vendor workflows.

03 · Local reinvention

Each market rebuilds the value story.

Global evidence is adapted repeatedly without clear boundaries around what is approved, what may change locally, what requires review, and what evidence supports each claim.

04 · Response discontinuity

Payer questions do not become organizational memory.

Questions, objections, evidence gaps, analyses, responses, commitments, outcomes, and market learning are often retained in local documents rather than reused globally.

How the solution works

Value evidence becomes one governed planning-to-response chain.

StromaOS coordinates evidence needs, methods, models, real-world analyses, claims, dossiers, local adaptation, payer and HTA response, commitments, and learning in one execution model.

STEP 01

Define the access question

Population, comparator, outcome, value claim, evidence gap, market requirement, payer objection, or HTA need.

STEP 02

Plan the evidence

Clinical, economic, epidemiological, real-world, patient, utilization, and market-specific evidence requirements.

STEP 03

Generate and validate

Models, analyses, cohorts, assumptions, scenarios, uncertainty, validation, review, and quality gates.

STEP 04

Assemble the value argument

Claims, evidence, model outputs, limitations, approved content, dossiers, and local adaptation boundaries.

STEP 05

Engage and respond

Payer and HTA questions, objections, analyses, commitments, negotiations, approvals, and follow-up.

STEP 06

Preserve and learn

Inputs, methods, versions, assumptions, decisions, responses, outcomes, commitments, and market learning.

Value evidence control

Every value claim remains connected to its methods, assumptions, evidence, and market boundary.

StromaOS preserves the full chain behind economic and access evidence: data inputs, cohort definitions, comparators, model structure, assumptions, utilities, resource use, scenarios, uncertainty, validation, reviewer decisions, and local adaptations.

Real-world analyses start from an approved cohort package, so the population a payer questions is the population your evidence team reviewed and approved.

Global teams can enable local execution without losing control of the evidence or approved argument.

Model a value evidence workflow
HEOR and market access work routed from evidence and model assumptions through analysis to an authorized value claim, under the Governance Spine.

Model assumptions, sensitivity and the approval that accepted them travel together. A payer challenge lands against a record, not a rebuild.

Governance throughout value evidence

AI can accelerate analysis and response without inheriting methodological or market authority.

StromaOS separates data preparation, analysis, modeling, interpretation, claim formation, local adaptation, drafting, review, approval, negotiation, and release.

Explore the Governance Spine
01

Method governance

Models, assumptions, cohorts, comparators, utilities, resource use, scenarios, validation, uncertainty, and reviewer acceptance remain part of the record.

02

Claim governance

Every value statement remains linked to approved evidence, model outputs, limitations, confidence, audience, jurisdiction, permitted use, owner, and review state.

03

Local adaptation control

Policy defines which global evidence elements may change locally, which require re-analysis, which require review, and which remain fixed.

04

Payer and HTA response authority

Drafting, scientific review, economic review, market review, approval, submission, negotiation, and commitment remain separate permissions.

05

Evidence Data Trace

Data, methods, models, prompts, assumptions, versions, reviews, decisions, claims, responses, commitments, and outcomes remain reconstructable.

Start with one evidence gap, economic model, dossier workflow, or payer response bottleneck.

Connect the evidence sources and specialist systems already in use. Define the method, assumptions, review, local adaptation boundaries, claim standard, and approval authority. Then run the work as one governed value evidence operation.