As a Digital Operation Platform for Life Science Industry, Taimei Technology has a wide range of services including Drug R&D, pharmacovigilance, pharmaceutical marketing and market access. With a full suite of self-developed software system line, we ave provided eCooperate(CTMS), eCollect(EDC), eArchive(eTMF), eBalance(IWRS), eVisit(ePRO), eImage-Medical Image Reading System, eSafety -Pharmacovigilance System, eSite-Clinical Trial Management System for GCP sites, eTrial - Phase I Ward System, eCollege-Training Management System and CRM System, etc. We also build an innovation platform TrialOS with the idea of cooperation, aims to realize the connection of the whole cycle of hospitals, pharmaceutical companies, the third-party providers, regulatory authorities, patients and other industry stakeholders. To achieve seamless data connection and smooth operation management, uniform industry standards and reach win-win success.
Through professional suites of software system, innovative cooperation platform and professional service capability, we teamed up with partners to deliver the unique comprehensive services of Clinical Trial Informationization, Pharmacovigilance, Independent Reading Committee, and SMO Collaborative Network.
At Taimei Technology, our mission is "Accelerating the Accessibility of Innovative Drugs”. We are establishing infrastructure for future 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 patients’ medical burden.
Since its founding in 2013, we have become the reliable partner for 600+ pharmaceutical companies, established partnership with 300+ third parties, connected directly with more than 300 hospitals, provided services to 3 million patients the. We are very honored to be awarded the National High-Tech Enterprise. And we are the audited supplier of CDISC and WHO-UMC. As the industry leading, our products have obtained certifications of ISO9001, ISO27001 and ISO20000-1, Grade III Certification of grade protection evaluation of the Ministry of Public Security and Trusted Cloud Enterprise SaaS Certification, and we take the lead in connection with National ADR Direct Reporting System.
1100+ a cross-border talent team from pharma and internet industries
400+ industry experts in product and RD team, most of them worked for top technology companies
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）
- ICH-E2B（Data Interchange Standard）
Qualifications of international certified vendor
- WHO-UMC certified vendor
- CDISC member and registered vendor
Docking with domestic and foreign regulatory agencies database
- Completed system docking with ADR direct reporting system