Our quality management system covers product research and development, production, inspection, sales, after-sales etc. The construction of the system is not only a mandatory requirement to ensure the market circulation of medical devices, but also an important mean to realize the full life cycle control of medical devices.
Tacro can provide advisory services of mutinational quality management system such as ISO13485, QSR820 etc., and standard quality control of medical equipment production. Assisting clients to sort out comprehensive management, research and development, production, quality, sales and after-sales, helping overseas clients recognize domestic quality management standard requirements of medical device production.
| Consultation and Guidance of Quality System | Medical device GMP advisory service |
| Medical device GSP advisory service | |
| QMS audit from second party | |
| On-site audit guidance | |
| Overseas inspection of medical devices | |
| QSR820 quality sysytem consulting | |
| ISO 13485 quality sysytem consulting |
