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. 


 

Life Science Field

Life Science

Focused on life sciences,with deep insights within clinical research and pharmacovigilance

Cloud

Technology-Enabled

Develop leading SaaS-based softwares with cloud computing, mobile and AI technology

Solution

Solution

Professional system + professional services
From planning to implementation of comprehensive coverage



Provider

Provider

Professional service
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

 



Our Milestones


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.

 MetInfo enterprise content manager system | MetInfo CMS



Our Mission


Website Keywords

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