Singapore Consults On Medtech UDI System
New UDI system to be enforced in biennial stages, starting in 17 months’ time
Singapore’s devices regulator is seeking comments on recently issued draft guidance on a medical device Unique Device Identification system.
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Singapore drives much of the medtech regulatory and policy thought leadership in the ASEAN region, as shown in its regulatory collaboration with Thailand and actions on cybersecurity and packaging waste.
Singapore Prepares UDI System, Malaysia Seeks Regulatory Improvements And Indonesia Adjusts To Changing Environment
Medtech industry representatives from ASEANMed member economies, notably Singapore, Malaysia and Indonesia, provided regulatory updates at the February Asia Regulatory Roundtable. These roundtables are organized by the ARQon consultancy and the Asia Regulatory Professional Association (ARPA). They are sponsored by Medtech Insight.
Medtech businesses in both Hong Kong and mainland China stand to gain from the Guangdong Hong Kong Macao Greater Bay Area plan, according to China’s medtech regulator, the NMPA.