From first-in-human to post-marketing, CRONCOX delivers integrated clinical research services with a sharp specialism in clinical data management and biometrics.
End-to-end ownership of your study database — from protocol-aligned CRF design to fully locked, CDISC-compliant data packages ready for analysis and submission.
SAS, R, and Python-based statistical programming delivered against CDISC standards. From sample size justification through submission-ready TLFs, our biostatistics team integrates with your protocol from day one.
Phase I through IV trial execution with rigor and pace. Our clinical operations team brings deep ICH-GCP expertise across feasibility, site selection, monitoring, and project management.
From protocol concept to submission dossier — our medical writers and regulatory professionals craft documents that withstand the toughest agency scrutiny across FDA, EMA, CDSCO, and PMDA.
Drug safety is a continuous obligation — and a regulatory minefield. Our pharmacovigilance team manages case processing, signal detection, and aggregate reporting with global compliance.
Beyond the clinical trial — we help sponsors generate evidence from the real world. Observational studies, patient registries, EHR analytics, and PRO instruments calibrated for regulatory acceptance.