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 200 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 20001 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.
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, 300+ 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
300+ 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 20001 IT Service Management Certification
Online WHO-DRUG coding system certified by WHO UMC
MedDRA medical terminology coding dictionary
WHO-Drug Drug Coding Dictionary