Digital Platform for
Life Science
We empower new drug research and development, and accelerate the process of new medicine and medical device launches through leveraging next generation digital research tools including Machine Learning and AI to automate labor intensive processes..
1000+
Customers
Database integration with regulatory agencies in 34 countries/regions
1400+
Staff
Worked with 21 of the top 25 Pharma companies
7000+
Clinical Trials
Our Solutions
Shorten Clinical Trial Study Start-Up Timelines up to 10x
eCollect(EDC)
Electronic Data Capture System
EDC system with remote data review and transparent data standards
eBalance(RTSM)
Randomization and Trial Supply Management
eBalance covers the subjects’ randomization, enrollment, drug supply & dispensation, emergency unblinding, and other processes, with real- time monitoring and management of medicine and trials.
eSAE
Safety Management in Clinical Trial Solution System
eSAE focuses on life-cycle SAE management from collection to archiving. It is based on one platform for SAE report management beyond safety database. Empowered by digital transformation, eSAE can reduce as much as 50% labor intensive efforts. Most important of all, it is compliant with GCP as well as GVP requirements.
We Deliver Solutions To Drive Success
The system of Taimei Technology has solved most of the problems in our TMF management, and the professional service team has saved us a lot of time in establishing the TMF structure and indexing.
Ann G. Vollmer
Clinical Research Manager, Lupeng Pharmaceutical US Clinical Team
Taimei Technology supports the construction and growth of our pharmacovigilance system. From the first cooperation guideline in 2015, it has helped us overcome many implementation difficulties.
Yan Zhang
Head of Pharmacovigilance and Quality, Pierre Fabre Pharmaceuticals (China)
To start from 0 to 1, we chose the CRO service. Now as the number of projects is gradually increasing, we decided build our own clinical trial system from database construction. Taimei’s EDC is exactly what we need at this stage.
Quangang Qu
Senior Director of Clinical Optimization, Roche Diagnostics
EDC System with Remote Data Review and Transparent Data Standards
01
AI AutomatedDatabase Design
AI-powered function that can parse the word descriptions in a trial protocol and convert them into eCRF structures for data collection in real time.
02
Customized ReportFor Any Purpose
Allows users to visualize data collected in a clinical trial into graphic reports, supporting all analytical and statistical needs from all roles.
03
Matrix Design & eCRFVersion Management
The matrix design shows a clear layout for users to assign forms to visits, and the eCRF version management to transfer collected data to a new version of eCRF.
04
Edit CheckAutomatic Testing
Our system can automatically test if all edit checks can run as expected with simulated data entry, and generate a test report.