Who Are We?

        As a leading technology solution provider in the field of life sciences, Taimei Technology is dedicated to propel biopharmaceutical industry development through state-of-the-art information technology, with focus in the field of clinical research and pharmacovigilance. 

        Taimei Technology provides the cloud platform for seamless clinical research collaboration between sponsors, sites, CROs, patients, regulatory agencies and third-party providers. On the foundation of our platform are 6 technology-enabled solutions encompassing data management, project management, electronic regulatory submission, central medical imaging, pharmacovigilance, and drug logistics. With biopharma industry drug development pain points in mind, Taimei Technology is dedicated to improving R&D quality and efficiency for accelerating innovation time-to-market while reducing costs. 

        Our clients include pharmaceutical enterprises, CRO and research institutes. To date, close collaborations and strategic partnerships with over 500 leading local and global pharmaceutical companies and CRO have been established. 

        Professional design philosophy and normative technical standards are the core principles of Taimei Technology product development, conforming to CDISC standard, Title 21 CFR Part 11 fundamental system standard and GAMP5 system validation standard. Taimei Technology is the first in the industry to obtain full-range ISO certifications, including ISO 9001 Quality Management Certification, ISO 27001 Information Security Management Certification and ISO 20000-1 IT Service Management Certification. Taimei Technology is also the first in various other aspects, including being a member and registered provider of CDISC, a WHO-DRUG system provider certified by WHO-UMC in China, first to establish FDA FAERS E2B gateway and first to establish gateway with Chinese National Adverse Drug Reaction Center.


Life Science Field

Life Science

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



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