Medical Devices EU Design Control Process Support

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.

NPD_process
We can support and guide trought all the develoment process.

Defining and addressing the User Needs, matching Technical possibilities to Business needs find best solutions and finally develop a successful product!

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