Pharmaceutical industry / clinical research
PRODUCTION ARCHITECTURE IN OPERATION

Coronis: Clinical
trials platform with
a unified information flow.

"From patient, medical and nursing staff to points of distribution - a unified data flow."
QUANTIFIABLE OUTCOMES ///

Operational Improvement Indicators

100%
Immediate update
Full recording and visibility at every stage of evaluation of the drug under study.
00,00 ms
Synchronization
Unified data flow between clinical and commercial management.
100%
Flexibility
The platform adapts to any level of clinical trial required.
DEEP ANALYSIS // SYSTEM ARCHITECTURE

A closer look at the transition.

Replacing the fragmented coordination of patients, staff, and distribution points with a single point of control. We designed and calibrated every step of this specialized need, using products from the Element ecosystem.

The Critical Problem:

Prior to Element, conducting clinical trials for new pharmaceutical formulations required coordination among patients, medical and nursing staff, and distribution points of the formulation under evaluation, without a single digital platform to connect them. Monitoring the progress of the drug’s evaluation and the interconnection with commercial/accounting management (ERP) was done fragmentedly, risking delays and loss of visibility in a process that demands absolute accuracy and traceability.

“Patients, staff, and distribution points operated separately, without a unified picture of the clinical trial’s progress.”

Implementation of "Element Custom Made" solution

We developed a management system for clinical trials of a new pharmaceutical formulation, connecting patients, medical and nursing staff, as well as formulation distribution points, into a single platform. The platform was interconnected with the business’s ERP, ensuring a unified data flow between clinical and commercial management.

The system allows real-time monitoring of the drug evaluation progress at all stages, giving Coronis a complete picture and control of the clinical trial from a single point – a solution tailored to the accuracy and compliance requirements that characterize the clinical research sector.

The platform is designed to adapt to whatever level of clinical trial is required each time.

CENTIVA EVALUATION

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