Digital Platform for
Life Science

Through digital technology solutions and innovative services, we empower new drug research and development, accelerate the process of new medicine launch for our customers, and improve business performance. Together, we will fulfill the vision of “building digital ecosystem for life science industry” for the benefit of patients.

Make good medicines within reach
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Provide technical solutions for 1000+ pharmaceutical companies/CROs

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Provide technical solutions for 7000+ clinical trials

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Database integration with regulatory agencies in 34 countries/regions



1400+ employees worldwide



3 major global market coverage (Asia Pacific, Europe, North America)


Electronic Data Capture System

EDC system with remote data review and transparent data standards

eCollect(EDC) - Electronic Data Capture System
RTSM - Randomization and Trial Supply Management


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.


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.

Pharmacovigilance​ - Holistic Services

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