Totrial's Intelligent Clinical Research System Applied in Medical Device Registration Clinical Trials

The Medical Device Registration Clinical Trial Researchers Conference led by Professor Gu Jun, Chairman of the Dermatology and Venereology Professional Committee of the Chinese Society of Integrative Traditional Chinese and Western Medicine, was successfully held in Shanghai. The system will be applied to this clinical study to realize real-time tracking and management of trial quality and progress through the interaction between electronic data collection and the clinical trial management system.

The clinical research intelligent monitoring system is a core architecture independently developed that covers six product lines such as DIP, EDC, and CTMS, covering the entire life cycle of clinical research. As a collaborative and efficient Internet product, it connects all parties with the project as the center, realizes real-time information sharing through data interaction and process collaboration, eliminates information gaps, improves data processing efficiency, and accelerates the experimental process.

The investigator meeting for a medical device registration clinical trial led by Professor Gu Jun, Chairman of the Dermatology and Venereology Professional Committee of the Chinese Society of Integrated Traditional Chinese and Western Medicine, was successfully held in Shanghai. Liu Xiaoai, Vice President of Totrial Group, was invited to participate in the discussion and showcased the group's self-developed new-generation intelligent clinical research system. This system will be applied to this clinical study, enabling real-time tracking and management of trial quality and progress through the interaction between electronic data collection and the clinical trial management system.

Totrial's clinical research intelligent monitoring system is an independently developed core architecture covering six product lines including DIP, EDC, CTMS, etc., covering the entire life cycle of clinical research. As a collaborative and efficient internet product, it connects all parties involved in a project with these parties at its core, achieving real-time information sharing through data interaction and process collaboration, eliminating information asymmetry, improving data collection and processing efficiency, and accelerating the trial process.

Among them, TT Capture (Intelligent Electronic Data Acquisition System) has obtained the Ministry of Public Security's third-level security certification, complies with international standards such as FDA 21CFR-Part11, and has assisted multiple products in passing NDA approval and marketing. TT CTMS (Clinical Trial Project Management System) complies with regulations from NMPA, FDA, and other countries, achieving standardized management of the entire project process (initiation, execution, monitoring, to conclusion), providing solid technical support for clinical research.