As a medical devices company in Asia, you want to expand your business and want to place your devices in Europe. TSQ Asia has collaboration with its mother company TS Q & E which can help you get your design approved in Europe. Some of the areas in which we can help:
- Design History File (DHF)
- Device Master Record (DMR)
- 510(k)
- Documentation
From Idealization to final market Introduction.
We are ISO 13485 certified for Medical Device Design, Development and all related activities.
