About Qualtech

YOUR BEST PARTNER IN ASIA

Qualtech is both a Medical Device Consulting Company and a Clinical Trial Organization (CRO), with a well-known reputation on regulation and product registration experience. Founded in 2000, Qualtech currently holds over 1,000 medical device licenses and has served over 1000 customers.

With abundant experience and international network, Qualtech can provide satisfying services and a one-stop solution for client's regulatory consulting, clinical trial, and marketing needs.

Qualtech operates in China, United State, Japan, Singapore, Taiwan, Malaysia, Philippines, Hong Kong, Indonesia and Vietnam. Every country has a dedicated team to provide our clients with local regulatory consulting, product registration and license holding services.

Qualtech Memorabilia

 

Establish Head Office in Taipei

2000
 

Establish Beijing Office; The 1st Consultant Obtaining TFDA GCP Approval

2008
 

Establish Singapore Office

2012
 

Establish HongKong Office

2013
 

Establish Malaysia Office

2014
 

TFDA GCP Approval

2015
 

Establish Philippines Office; Get China FDA GCP Approval

2016
 

Establish Japan Office and Indonesia Office; Get China FDA GCP Approval

2017
 

Establish Vietnam Office; Get China FDA GCP Approval

2018
 

Establish New Office, Taiwan GDP Enterprise

Establish Thailand Office and United States Office Become the 1st batch of Taiwan GDP verified enterprise

2019