Taiwan Starts the Priority Review of the Medical Device Registration - January, 2017
- 2020-02-15 06:43:35
On Nov 19th, 2013, the investigator meeting was held to start the clinical trial of Dermal Filler, a class III medical device, for CFDA registration purpose
MoreQualtech was invited by OMETA (Overseas Medical Eauipment Tech. Assistants) to give the speech of regulatory registration in Taiwan and China.
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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