Who Are We?
As a leading provider of technology-enabled solutions in life sciences, Taimei Technology aims at empowering our clients across pharmaceutical R&D, pharmacovigilance, marketing and market access with the comprehensive professional software product suite and technology-based professional service system. Our comprehensive software product suite includes eCooperate(CTMS), eCollect(EDC), eArchive(eTMF), eBalance(IWRS), eVisit(ePRO), eImage, eSafety, eSite, eTrial, eCollege, CRM, to name but a few.
Led by the core concept of “cooperation”, our TrialOS drug R&D cooperation platform integrate stakeholders from pharmaceutical enterprises, GCP sites, providers, regulators, patients to other stakeholders. We are poised to advance the value upgrade and realize a win-win situation for all parties by leveraging resource integration, data interaction, process cooperation and standard unification.
With the application of advanced technologies such as artificial intelligence, Taimei Technology provides clinical trial data management, biostatistics, independent reading committee and pharmacovigilance services to our clients. By equipping with the professional software suite, TrialOS platform, professional service capability and data-driven evidence, Taimei Technology work closely with our strategic partners to provide total solutions in clinical research and pharmacovigilance.
Guided by our mission of accelerating the accessibility of innovative drugs, Taimei Technology is forming the infrastructure for the future development of pharmaceutical industry. Our goals are to accelerate the process of new drug R&D, improve drug accessibility, ensure patients’ safety use of drugs and reduce the patient's medical burden.
Today, Taimei Technology has become the reliable partner for more than 500 leading pharmaceutical companies and CROs in China and abroad and cooperated with 1,600+ hospitals. The TrialOS platform supports 1/3 of China's registered clinical research and 1/5 of ADR submission.As the first enterprise to access National ADR Direct Reporting System and complete system docking with FDA FAERS and EudraVigilance, Taimei Technology has product service suite is authorized by ISO Certifications, Class III information system security protection of the Ministry of Public Security and certification of Trusted Cloud, enterprise-class SaaS Evaluation. Taimei Technology is also the National Hi-Tech enterprise and certified vendor of CDISC and WHO-UMC.
Focused on life sciences,with deep insights within clinical research and pharmacovigilance
Develop leading SaaS-based softwares with cloud computing, mobile and AI technology
Professional system + professional services
From planning to implementation of comprehensive coverage
Real-time support, fast response
Professional service from professional team
In Taimei Medical Technology, 700+ staff are committed to providing you professional services based on our
over 15 + years of professional experiences in the industry.
40% + employees are quipped clinical research or pharmacovigilance experience
700+ staff 15 + years of professional experiences 40% employees from healthcare industry
Committed to the application of state-of-the-art technology in healthcare, we are constantly developing a series of leading products based on cloud computing, mobile and AI technology.
We are specialized in software design, production, implementation and consulting to improve the efficiency and quality of the industry.
Accelerate New Drug Time-To-Market and Advance Life Sciences
Leading the Industry with Strict and Compliant
Product Design Standards
Validation in compliance with industry standards
Title 21 CFR Part 11 (International Basic Standards)
CDISC (Data Interchange Standard)
GAMP5 (System Verification Standard)
The first CDISC member and registered supplier in China
The first in the industry to fully pass all certifications
ISO 9001 Quality Management Certification
ISO 27001 Information Security Management Certification
ISO 20000-1 IT Service Management Certification
Online WHO-DRUG coding system certified by WHO UMC
MedDRA medical terminology coding dictionary
WHO-Drug Drug Coding Dictionary