data analytics

With the application of powerful and insightful data analytics functionality across administrative, operational and clinical functions, stakeholders can now identify, action and resolve the potential issues detected before they  negatively impact the trial.

eco-system

Clinical Trials Intelligence has created an eco-system that fosters collaboration across the entire pharmaceutical industry while addressing the privacy and security concerns of all stakeholders.

clinical data

A “first of it’s kind” perpetually increasing library of clinical data analytics that facilitates the sharing of “lessons learned” across corporate boundaries without any compromise of sensitive data.

workflow management

Advanced workflow management, including “closing the loop” functionality and a blockchain based immutable audit-trail.

CTi-OEM

Operational Excellence

Provides intuitive operational oversight of clinical trials for clinical project managers, clinical data managers and remote staff, allowing instream decision-making on what actions are required to ensure a successful project.

CTi-CDV

Clinical Data Visualisations

Provides enhanced clinical data review through the use of data visualisations to identify issues that may impact on the trial integrity and safety of the patient e.g. data quality issues, disease exacerbation. Furthermore, CTi-CDV will facilitate flagging of these issues, and corrective actions to be recorded and monitored.

CTi-PDA

Predictive Analytics

The CTi-PDA application will combine all operational and clinical data sources and use predictive modelling to forecast issues and events before they happen. The CTi-PDA application will reveal hidden correlations across all datasets thereby facilitating the pharmaceutical company to take pro-active action to address.

CTi-RBM

Risk Based Monitoring

The CTi-RBM application will use current and historical data to predict specific risks, and thereby allow for tactical deployment of the pharmaceutical company’s data and site monitoring resources to take preventative action. This predictive risk based approach differs from current reactive approaches to risk and can significantly reduce site monitoring costs during a clinical trial.

CTi-PRR

Patient Recruitment and Retention

The CTi-PRR application manages recruitment and retention of patients for clinical trials by providing a portal for patient identification and producing a series of alerts (based on predictive analytics) that flag when a patient is at risk of withdrawing from the study.

CTi-SIM

Site Investigators

The CTi-SIM application manages the recruitment of investigators (physicians) to run clinical trials,and manages token payment compensation by the pharmaceutical company to investigators, triggered by data-driven milestones and KPIs, defined on Clinical Trials Intelligence.

CTi-VMM

Vendor Management

CTi-VMM provides oversight on data quality and manages token payment compensation by the pharmaceutical company to the third party vendors, triggered automatically by data-driven milestones and KPIs, defined on Clinical Trials Intelligence.