THE CENTER OF EXCELLENCE FOR CLINICAL TRIAL DATA
Originally established as a specialist biometrics Contract Research Organization, CROS NT remains a data centric CRO providing services globally from feasibility to clinical study report for Phases I-IV and medical device trials. CROS NT’s contribution usually starts in early phase development where we support with expert clinical and statistical study design and regulatory consultancy. We provide “consultancy with deliverables” such as protocols, evidenced based feasibility, regulatory plan, and an outsourced monitoring solution.
Services include data management, biostatistics programming & analysis, pharmacovigilance and medical writing – and accompanying eClinical applications (EDC, CTMS, IWRS, ePRO) for all phases and medical device studies. We offer a center for Sponsors’ clinical data across a program of studies, facilitating excellent data visualization, risk based monitoring, meta-analysis, standardization, traceability and efficiencies that substantially reduce costs. All services are underpinned by strong clinical and biometrics project management.