Trial Data OS
DCT Operation System


Quick Search:
Users can search by study drug, tumour classification, study phase, study investigator, project name to quickly search for clinical studies and view project details
Smart Matching:
Users can enter the disease information and the system will intelligently match and recommend the suitable clinical study
Online Consultation:
Users can initiate an online consultation with a professional doctor to obtain professional information feedback
Project Registration:
Users can submit project registration materials online for their intended projects, which will be reviewed online by professional clinical investigators, and the off-line follow-up process will be seamlessly connected to the subjects who meet the preliminary screening conditions
Trial Data cooperates with the National Cancer Center to provide cancer patients with authoritative and professional tumor clinical trial project inquiry,consultation and registration support.Effectively improve the efficiency of patient recruitment for tumor clinical research projects and accelerate the clinical research process.
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Easy to use:

No geographical restrictions, subjects can give informed consent at home Transparent and traceable informed process Real-time communication between investigator and subject with fully informed process to effectively protect the rights of subjects

Convenient for everyone:

Support both on-site and remote clinical studies Ensure the use of correct version in each site Quickly notify and sign the updated version of ICF
Trial Consent is a subject-centric eConsent tool. Use plain language and multimedia interaction (photos, videos, etc.) throughout the study, which allows the subjects to quickly and fully understand the study, making the subjects feel more involved. At the same time, it can also ensure that the subjects are fully informed by the investigators.


High Convenience:
e-Visit system is designed based on WeChat portal, no need to download APP
High Data Quality:
Real-time data page quality control and three-level reminder function to ensure data quality
Easy Interaction:
The system effectively links subjects, CRC, and invetigators to facilitate the interactive communication according to the project progress, realizing comprehensive information synchronization and online management throughout the entire process
Good Experience:
e-Visit is easy to use and equipped with clear task management, integrated AI image and voice recognition. The system can complete various out-of-hospital data collection requirements such as subject logs, medication logs, discomfort records, scale questionnaires, smart wearables, etc.
  • e-Visit out-of-hospital data collection system is based on mobile internet technology and enables the intelligent and efficient collection of out-of-hospital data from the subject's smartphone terminal.
  • Simple calendar-style task display and smart reminder function improve user experience.
  • Convenient online interactive features, progressive filling mode and game-based guidance to stimulate subjects' interest in participation and to improve compliance. Effectivly reduce subject dropout rate.
After randomization, the system automatically generates a drug dispensing application, which is reviewed and confirmed by the investigator and then dispatched by the central warehouse for direct delivery to the subjects' homes through logistics. One system can achieve the whole process of drug management through drug application, approval to logistics order, order acceptance, delivery tracking and receipt confirmation.