On August 25th 2017, Professor Xi Ting-fei from Peking University visited Qualtech Taipei Headquarters. Professor Xi Ting-fei is the director of Biomedical Material and Tissue Engineering Research Center of Academy for Advanced Interdisciplinary Studies, Peking University.
More Last August 1, 2017, in line with Qualtech bringing its services closer to clients, a business office was opened in Japan. The new office offers medical device regulatory research and consultancy for product registraiton, local representation and clinical trial services in China, Taiwan and ASEAN to our Japanese clients
More Industry Facts: 27-28 November 2017Philippines positioning itself as a leader in healthcare outsource services.
Hong Kong Trade Development Council: The Philippines: Market Profile
The Government of India notified in February 2017 the new Medical Device Rules 2017, which will come into force starting January 1, 2018. The new Rules have been framed in conformity with Global Harmonisation Task Force (GHTF) framework and conform to best international practices.
More On September 4th 2017, China Food and Drug Administration (CFDA) officially published the new revision of "Medical Device Classification Catalog". It will be implemented from August 1, 2018
More Medical Tourism in Southeast Asia: Indonesia's Opportunity Cost. (n.d.). Retrieved July 28, 2017
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