International Clinical Trial Institution Management Platform
ClinCluster® is an innovative international clinical trial site management platform, currently piloting clinical trial sites in the Greater Bay Area. Combining project oversight and system oversight, it ensures smooth, consistent, and efficient clinical trial operations across all ClinCluster® sites. ClinCluster® enables institutions to manage their work and clinical trial planning processes using the same standards and methodologies. ClinCluster® also enables remote audits and inspections, facilitating the work of applicants and regulators. It focuses on high-risk factors, reduces their time spent on-site, and implements the risk management principle of proportional to risks and importance as outlined in ICH GCP (R3).
Project Oversight
Single point of coordination
ClinCluster® professionals coordinate the trial project
Contract & Budgets
Accelerate clinical trial implementation with unified contract templates and standardized financial budgets
System Oversight
Harmonized SOPs
To ensure the quality of clinical trial implementation,
the quality management system of ClinCluster® member institutions will be uniformly constructed.
Personnel Training
Provide personnel training for institutions,
covering basic GCP and research ethics, clinical trial operations and management
Clinical Trial Institution Management Electronic Cloud Service Platform
ClinCluster® utilizes digital tools for management. Each participating clinical trial institution is granted access to eCPort®, a cloud-based platform specifically developed for ClinCluster®. Designed with users and trial processes in mind, eCPort® adheres to regulatory compliance standards, is computer-verified, and utilizes cloud technology, eliminating the need for server-side integration. eCPort® can be used by multiple institutions simultaneously, allowing users to access and monitor their work online anytime, anywhere.