Taiwan Starts the Priority Review of the Medical Device Registration - January, 2017
- 2020-02-15 06:43:35
More and more regulatory had been set up and released in ASEAN countries recently.
MoreThe Asia Regulatory Professional Association (ARPA) is an organization of Healthcare Regulatory Affairs professionals in Asia. ARPA aims to raise the standard and social recognition of Regulatory Professionals as part of Healthcare team. QT has the honor to invite ARPA to the conference in Taipei Technology University every year.
MoreAssociation of Southeast Asian Nations (ASEAN) is composed of 10 countries in Southeast Asia. It’s the market with good potential for someone who would like to build a stance in the market of medical devices.
MoreQualtech TFDA manager is invited to be the speaker in Singapore seminar "Understanding Taiwan's Regulatory Framework for Medical Devices" organized by Singapore Manufacturing Federation and DH RegSys Pte Ltd.
MoreQualtech was invited by OMETA (Overseas Medical Eauipment Tech. Assistants) to give the speech of regulatory registration in Taiwan and China.
MoreThe successful forum had been held on April 15th, 2013 at Taipei.
MoreThailand’s Ministry of Public Health has announced a set of medical device definition for manufacturers and importers to follow when registering their medical device according to risk-based classification, to gradually endorse the transition of Thailand away from policy-based classification.
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