Real-World Evidence. Quality at Half the Time.

Retrospective studies, comparative effectiveness, registry design, and pharmacovigilance, evidence beyond clinical trials.

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Trusted by over 200,000+ researchers

Trusted by over 200,000+ researchers

Trusted by 200,+ institutions and individuals

Trusted by 200,000+ institutions and individuals

50%+

Faster Than Traditional CROs

30+

Data Source Integrations

95%

Extraction Accuracy

STROBE

Compliant Outputs

Solutions

Built for the RWE team's actual day.

Database Studies

Claims-based and EHR analyses of treatment patterns, outcomes, resource use, and costs.

Comparative Effectiveness

Propensity-score matching and causal inference comparing products in real-world settings.

Registry Design

Prospective patient registries with protocols, CRFs, SAPs, and data management specs.

Pharmacovigilance

Post-authorisation safety studies, adverse event profiling, and signal detection.

Epidemiology

Incidence, prevalence, and disease burden analyses for market sizing and unmet need.

Publication-Ready

STROBE-compliant manuscripts and evidence packages for regulatory submission.

Processes

Every Step Traceable

Five steps, one workspace, every method traceable

Step 01

Design

Protocol and SAP developed together. Endpoints, comparators, data sources, and causal inference methods defined before a single query runs.

Step 02

Source

Claims, EHR, registries, or new prospective collection. Data feasibility assessed against the research question, not the other way around.

Step 03

Analyse

Causal inference executed with the right method for the question. Sensitivity analyses and robustness checks run automatically alongside the primary model.

Step 04

Validate

Clinical and statistical review built into the workspace. External validity comparison, QC flags, and peer-review prep in one place.

Step 05

Publish

STROBE-compliant manuscripts, regulatory packages, and executive summaries. Every figure, table, and claim source-linked to the analysis behind it.

Deliverables

Why RWE Teams Work Here

Same quality. Half the time

The rigour of a specialist RWE CRO, delivered on your team's timeline. Propensity matching, IPTW, and sensitivity analyses run in days, not sprints.

Same quality. Half the time

The rigour of a specialist RWE CRO, delivered on your team's timeline. Propensity matching, IPTW, and sensitivity analyses run in days, not sprints.

Same quality. Half the time

The rigour of a specialist RWE CRO, delivered on your team's timeline. Propensity matching, IPTW, and sensitivity analyses run in days, not sprints.

Every assumption, documented

Every inclusion rule, covariate choice, and method decision recorded as the analysis runs. Reviewers and regulators see exactly why every call was made.

Every assumption, documented

Every inclusion rule, covariate choice, and method decision recorded as the analysis runs. Reviewers and regulators see exactly why every call was made.

Every assumption, documented

Every inclusion rule, covariate choice, and method decision recorded as the analysis runs. Reviewers and regulators see exactly why every call was made.

One platform. Every method.

Claims, EHR, registry, and survey analyses in the same workspace. No switching between SAS, R scripts, and a separate dossier writing tool.

One platform. Every method.

Claims, EHR, registry, and survey analyses in the same workspace. No switching between SAS, R scripts, and a separate dossier writing tool.

One platform. Every method.

Claims, EHR, registry, and survey analyses in the same workspace. No switching between SAS, R scripts, and a separate dossier writing tool.

Publication-ready from day one

Manuscripts drafted directly from the locked analysis. STROBE checklist complete, figures exported, references in place. Submission-ready without a rebuild.

Publication-ready from day one

Manuscripts drafted directly from the locked analysis. STROBE checklist complete, figures exported, references in place. Submission-ready without a rebuild.

Publication-ready from day one

Manuscripts drafted directly from the locked analysis. STROBE checklist complete, figures exported, references in place. Submission-ready without a rebuild.

Why Access Teams Are Switching to AnswerThis

RWE Study Reports

Full reports with protocol, methodology, statistical analysis, results, and interpretation. Ready for internal review or external audit.

Treatment Pattern Analyses

Prescribing, adherence, persistence, and discontinuation in routine care. Exportable tables, publication-ready figures.

Treatment Pattern Analyses

Prescribing, adherence, persistence, and discontinuation in routine care. Exportable tables, publication-ready figures.

Healthcare Cost Studies

Real-world cost and resource utilisation analyses. Structured to feed directly into economic models and HTA submissions.

Healthcare Cost Studies

Real-world cost and resource utilisation analyses. Structured to feed directly into economic models and HTA submissions.

Registry Documentation

Protocols, CRFs, SAPs, and data management plans for prospective registries. Built to regulatory specification.

Registry Documentation

Protocols, CRFs, SAPs, and data management plans for prospective registries. Built to regulatory specification.

Ready to get started

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AI-powered evidence generation for life sciences. Structured literature reviews, HEOR, market access, and reimbursement strategy — delivered end-to-end.

Services

Systematic literature review

HEOR & Economic Modeling

Market Access

Reimbursement & Payer Dossiers

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