Medical Device Registration

Registration

The major medical device market countries in the world have relevant regulatory requirements for the listing of medical devices. Applicants who want to sell medical products locally need to obtain relevant product certificates from local healthy ministry.
Qualtech has more than 20 years of registration experience in Asia and has set up local offices in as many as 11 countries. We can assist your products to be quickly listed locally.

Pre-clinical test

Qualtech provides a one-stop solution for testing and registration, using our regulatory experience to formulate a suitable test plan for your product.
We provide relevant pre-clinical tests, including biocompatibility, immune tests, virus tests, sterility tests, animal tests, electrical safety, software validation and other relevant international standards.

Regulatory Research

We have a professional and diverse regulatory team that can produce local regulatory research reports according to your needs, helping your company better understand the relevant regulations of the local government on medical devices in order to facilitate market advancement.

WHY CHOOSE QUALTECH?

An Excellent Management System to Ensure Time-efficient Project Handling.

Qualtech Operates Locally through our Subsidiaries in Every Serviced Country.

Expert Teams with Extensive Experience to Strongly Support Your Project.