CRONCOX partners with sponsors and biotechs to design, build, and manage clinical trial data with precision — from first-in-human studies to global Phase III programs.
End-to-end study database design, EDC build, edit checks, query management, and database lock — delivered against CDISC standards.
Learn more →SAS, R, and Python programming. SDTM, ADaM, and TLF outputs ready for regulatory submission. Statistical analysis plan to CSR.
Learn more →Site selection, monitoring, project management, and feasibility for Phase I–IV trials in compliance with ICH-GCP.
Learn more →Protocol authoring, ICF, clinical study reports (CSR), and submission-ready dossiers for FDA, EMA, CDSCO, and PMDA.
Learn more →Drug safety monitoring, SAE management, MedDRA / WHODrug coding, and aggregate safety reporting (PSUR, DSUR).
Learn more →Observational studies, registries, and RWD analytics from EHRs, claims data, and patient-reported outcomes.
Learn more →We're not the biggest CRO in the world — and that's the point. CRONCOX combines the rigor of a big-pharma quality system with the agility, transparency, and partnership of a true specialist. Your study isn't one of hundreds in our pipeline. It's the one we're building.
Discovery session, feasibility review, and proposal aligned to your protocol, timeline, and budget.
Study database design, DMP authoring, CRF specification, and CDISC-aligned data model build.
Live database build, edit check programming, UAT, and study go-live with continuous data review.
Database lock, SDTM/ADaM packages, CSR support, and full archive transfer to sponsor.