Integrated remote management platform for clinical trial monitoring, auditing, and verification, empowering digital trials and enhancing competitiveness
Hybrid monitoring is the new standard in clinical trials, reducing on-site visits, enhancing quality control, and providing real-time insights while lowering labor and travel costs, paving the way for fully integrated trial platforms
Integrate clinical data from HIS, LIS, EMR, PACS, medical records, prescriptions, nursing notes, and pathology reports
Provide a comprehensive, panoramic view of every trial participant’s clinical trial journey
CRCs can capture and upload via PDA, with de-identified storage for efficient management of original paper data
Trial documents are uploaded in bulk using high-speed scanners, simplifying file management and reducing storage load
Pre-set QC rules based on the clinical trial protocol to automatically flag and record issues like prohibited medications, concomitant drugs, and SAEs for timely feedback
Locally deployed systems ensure security and stability, keeping data within the hospital
Monitoring staff can apply for remote monitoring, with institutional approval and local management
Comprehensive technical support and system training ensure smooth deployment and operation
Compliant with China’s Personal Information Protection Law, with strict data de-identification to prevent privacy breaches
Facial recognition prevents unauthorized access, and the system detects risky behavior, issuing alerts or forced shutdowns
Real-time watermarks protect against screenshot leaks
VPN access control with full audit trails ensures data security and compliance
Comprehenssive monitoring records provide traceability and transparency
-A nationwide remote monitoring network is taking shape-
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