Case studies · Hub

What this data can actually support, and where it stops.

Six worked examples of the questions Asia-Pacific real-world data can answer, the shape of the work behind each, and the limits that apply. Then the published literature that establishes, independently of us, what this region's data can support.

These six are illustrative. They are composite examples built to show the shape of the work, the data types involved and the constraints that apply, not descriptions of specific client engagements. We do not publish client names, and we will not publish yours. Where a real engagement is discussed, it happens under NDA in conversation, not on a website.

Illustrative case studies

Six questions, and what it takes to answer them.

Different questions need different data. The matrix below shows which types carry the weight in each of the six, before the detail underneath.

QUESTION Claimsgov / insurer EMREHR Hospitalactivity Dispensing Labresults Registrybiobank Linkeddata Unmet need, sized Real standard of care Evidence a payer accepts Where the volume is Rare disease, findable? Biomarker cohort exists? Primary source Supporting source Availability differs by market. This is the shape of the answer, not a promise about yours.
Illustrative

Where is the unmet need, and how big is it?

The question. A medical affairs team needs to size the population still cycling through therapy lines without reaching a durable response, before committing to an evidence programme.

The shape of the work. National claims plus dispensing, in a market with near-universal coverage. Define lines of therapy from dispensing sequences, identify switching and discontinuation, and quantify the group that exhausts available options.

Where it stops. Claims record what was funded, not why it was stopped. Discontinuation is inferred, not observed, and the analysis must say so.

Illustrative

What does standard of care actually look like here?

The question. A clinical team designing a regional trial needs the real comparator arm, not the guideline one.

The shape of the work. Hospital and EMR data in two markets, harmonised by one written specification and executed locally in each. Extract observed first-line regimens, sequencing and time-to-next-treatment.

Where it stops. The two markets cannot be joined at the record level. Results are compared as summaries, with an explicit statement of where the comparison stops being defensible.

Illustrative

Will the payer accept this as evidence of value?

The question. A market access team faces a submission deadline and needs to know whether local data can produce the burden-of-illness evidence the HTA body expects.

The shape of the work. A feasibility read first: is the cohort identifiable, is the cost captured, is the follow-up long enough. Then a costed utilisation analysis against the HTA body's own stated evidence requirements.

Where it stops. If the follow-up window is too short for the endpoint the payer wants, no analysis fixes it. That is a finding, and it is cheaper delivered in week three than month six.

Illustrative

Where is the volume, and who is treating it?

The question. A commercial team needs to know which hospitals actually deliver a procedure, at what share, and how that has moved, to target field effort properly.

The shape of the work. Published hospital activity data, segmented by procedure, ranked by hospital, with share of national and share of state. In Australia this is a Health Grid Platform view rather than a project.

Where it stops. Activity data shows what was done, not what it cost the hospital or how it was decided.

Illustrative

Is this rare disease population even findable?

The question. A rare-disease team needs to know whether a defensible incidence figure exists in a region where the condition has no dedicated registry.

The shape of the work. A landscape assessment across three markets: which coding systems capture the condition at all, whether a claims-based case definition can be validated, and whether an existing epidemiological cohort is faster than building one.

Where it stops. Sometimes the answer is that the population cannot be identified reliably from routine data, and primary research is the only honest route. We say so.

Illustrative

Does the biomarker-defined cohort exist in this market?

The question. A precision-medicine programme needs to know whether testing rates are high enough for a biomarker-defined cohort to be assembled locally.

The shape of the work. Laboratory results linked to clinical records in a market where genomic and clinical data sit close together. Establish testing rate, positivity, and whether the tested population is representative.

Where it stops. If only a selected subgroup is tested, the cohort is biased by construction, and the size of that bias has to be stated, not buried.

What all six have in common

Five things that are true of every engagement.

01

The feasibility read came first

In writing, before money. In two of the six, it changed the question. That is the read doing its job.

02

The cohort specification was approved before analysis

Dated and signed. This is where most projects are saved or lost, and it is not a formality.

03

The limitations were written down at the start

Not discovered in review. A limitation you predicted is a caveat; one you did not is a finding against you.

04

Nothing left the country

Records were de-identified at source by the local alliance partner and analysed in-market inside a controlled-access environment, under that market's own law.

05

Multi-market meant harmonisation, not linkage

One written specification executed locally in each market, with summary results compared, and a published position on where the comparison stops.

The independent record

What the published literature establishes about this region.

The examples above are ours. The following is not, it is the public record of what Asia-Pacific real-world data has been shown to support, established by researchers with no connection to this firm.

Cross-market pharmacoepidemiology is established practice

Multi-country studies across Asian health systems have been conducted and published, demonstrating that harmonised protocols executed locally can produce comparable results.

Real-world evidence already informs reimbursement in Asia

Published reviews document real-world data being used to support drug reimbursement decision-making across Asian markets, it is not a theoretical use case.

Cross-regional data initiatives exist and function

Collaborative initiatives spanning regions have assessed treatment and development questions using linked and harmonised health data.

These publications are cited as evidence about what real-world data in this region can support. They are not evidence about Aurumetrics. Aurumetrics is not a member of, does not participate in, and has no data access through any network, consortium, working group or initiative described in them. The authors and institutions cited have no association with Aurumetrics and have not reviewed or endorsed this page.

Which of these is closest to your question?

Describe it in a sentence or two and we will tell you whether the data can answer it, in which market, and how long it would take.

De-identified patient-level data and publicly available data, through local alliance partners. De-identification at source. Analysis in-market, under local law. Never identifiable records.