Case Study: Global CRO (Pharmaceutical & Biotech Industry) achieves integrated, compliant clinical and pharmacovigilance management with ArisGlobal

Global CRO chooses ArisGlobal to manage Clinical and Pharmacovigilance

Global CRO Pharmaceutical and Biotech Industry, a UK‑headquartered international full‑service CRO with strong oncology and rare‑disease expertise, faced fragmented third‑party EDC tools that lacked the cohesiveness, flexibility and proven EDC–CTMS integration needed across its global offices. Seeking a single‑vendor partner able to support electronic, paper and hybrid studies, ensure regulatory compliance, and reduce vendor management overhead, the CRO evaluated ArisGlobal’s agCapture (EDC) alongside its existing agClinical (CTMS) and selected ArisGlobal as its clinical technology partner.

ArisGlobal implemented on‑premise agCapture integrated with agClinical, collaborating closely with the CRO to configure and rebrand the systems, automate study setup and site workflows, and provide TMF functionality, IWRS/randomization and multi‑lingual support. The result was faster, more consistent study setup and execution, improved operational visibility and regulatory compliance, simplified vendor management, and the ability to monitor studies across 30+ countries — outcomes the CRO attributes directly to its partnership with ArisGlobal.