Clinical path
Biometrics without the theatre.
Emerging and mid-size sponsors do not need a 200-person CRO. They need a programming studio that has done ADaM, lock, and CSR, and will still be on the call when the agency writes back.
From protocol to questions
Data management, statistical programming, study reporting, RWE and HTA support — taken as a cluster or as a single workstream.
CDISC as a habit
SDTM and ADaM are not a conversion we bolt on at the end. They are how the study is built, so the CSR and the dossier do not fork.
A studio, not a queue
You get a named lead. Our bench is small on purpose. If we are full, we say so.
Services on this path
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.
Real World Evidence
Study design, programming and analysis of real-world data that a medical affairs or HEOR team can defend.
Health Technology Assessment
Evidence packages and analyses that market-access teams can take into HTA and Joint Clinical Assessment.
On-Demand Service
Named programmers available on a short fuse — a TLF wave, a lock, a model sprint.
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.