Prepare reimbursementsubmissions faster.
AI drafts HTA submissions, pricing briefs, and payer responses from your existing evidence—with sources attached for expert review.
For HEOR, HTA, Pricing & Global Market Access teams.
Early-access pilots · Platform in development
Keep reimbursement work
on schedule.
Draft the dossier, prepare local versions, and answer evidence questions from the same source documents.
Get the global dossier ready sooner.
AI drafts your value dossier from study reports and literature, with supporting sources attached for review.
Example Draft the comparative-efficacy section from the study report, keeping the comparator, population, and follow-up explicit.
You provide
Study reports, published evidence, and your dossier template.
You receive
Draft value-dossier sections, payer narratives, and source links.
Measure the change
Days to internal sign-off; total drafting and review hours.
Synthetic examples. Pilot scope and expert review are agreed in advance. JCA clinical work, national economic work, and new analyses are scoped separately.
Catch errors
before submission.
Check claims, figures, and references across the dossier, model documentation, and payer materials before final sign-off.
Find conflicting figures.
Compare patient counts, data cuts, currencies, and assumptions across documents.
Check what supports each claim.
Open the source passage behind a claim and flag missing support.
Focus review on changed sections.
See which claims and sections need review when an input changes.
The dossier and model use different eligible populations.
The dossier defines adults after one prior line of therapy. The model’s input sheet includes the broader indicated population.
ILLUSTRATIVE EXAMPLE · NOT CLINICAL EVIDENCE
Measure the
time saved.
Start with one dossier section, market adaptation, pricing brief, or assessor response and compare time to sign-off with your current process.
Start with the evidence you already have.
Use your existing evidence.
Start with your study reports, dossiers, templates, and model outputs; we agree an editable deliverable and review criteria before work starts.
Keep your experts in control.
Your team approves methods, interpretation, model outputs, and final wording; new analyses, model development, and regulatory submission publishing are separate scopes.
Start with a scoped pilot.
The platform is in development, and we are scoping AI-enabled service pilots with agreed outputs, review responsibilities, timing, and fees.
Discuss the work before sharing files.
Initial scoping can use public or synthetic material; confidential documents require an agreed contract and data-handling review.