RWD · epidemiology
Evidence from the world as it is.
RWE only works if the data, the design and the programming agree. We help frame the question, build the cohort, and produce analyses that HEOR, medical affairs and regulators can actually use.
Who it's for
The brief we take.
HEOR, medical affairs, and biostatistics teams who need RWD programmed with the same QC culture as a CSR — not a one-off notebook.
Deliverables
What leaves the studio.
- Protocol and SAP support for observational studies
- Cohort construction and sensitivity analyses
- Propensity, survival and regression modelling
- Reproducible R and SAS pipelines
- Tables and figures for publications and dossiers
- Data-source feasibility notes
Tools & standards
The stack, without the logo wall.
Engagement
How you hire us.
- End-to-end observational study
- Analysis-only on a cohort you already hold
- Publication graphics and QC
Anonymized: external-control arm analysis for a rare-disease filing, with pre-specified sensitivity set and a programmer's appendix for the agency.
FAQ
Before the call.
Do you license claims or EHR data?
We do not sell data. We work on datasets you license or generate, and we will tell you early if the source cannot answer the question.
Also in the studio
Statistical Programming
Submission-ready analysis datasets and TLFs, programmed once and QC'd twice.
Clinical Study Reporting
CSR sections, appendices and in-text tables written to the numbers — not around them.
Data Management
Clean, lockable clinical databases with CDASH-minded eCRFs and a query process that does not stall sites.
Tell us what is on the clock.
A scoping call is thirty minutes. Bring a protocol, a TLF list, or a model that needs hands.