ClinQuick®

Celerion’s proprietary esource system

Enabling faster, more accurate data acquisition

Developed to address the most challenging aspects of data collection, data management and clinical operations, ClinQuick is Celerion’s industry leading eSource solution. ClinQuick is a CFR Part-11 compliant barcoded system that automates all aspects of clinical operations. This ensures that we can provide faster delivery of high quality data, benchmark level study execution times and consistent execution of clinical trials across Celerion’s global facilities.

Fully Automated Data Management

By integrating ClinQuick with TrialMaster, we’ve created a fully automated clinical data management platform that combines both data management and reporting into a single, centralized database. This unique capability helps reduce costs through remote monitoring, automated query management and real-time edit checks.

Integrated Clinical Instruments

ClinQuick is integrated with clinical and laboratory equipment, reducing errors by omitting the need for data transcription and enabling high quality data to be captured directly.

See Your Data Online, in Real Time

ClinQuick’s integration with Celexus makes it possible to see the results of your drug's trial in real time online, as we collect data at the study sites or in our lab.

Make Earlier Go / No-Go Decisions

Because ClinQuick electronically captures data in real time, study specific criteria is prebuilt into each study, ensuring faster quality review leading to earlier informed decisions about your drug's future.