Understanding Taiwan’s Regulatory Framework for Medical Devices

25/06/13 - 26/06/13

During the two days event, participants were introduced to the Regulatory Framework for Medical Device in Taiwan and the regulatory body who ensures medical devices are regulated to meet quality, safety and efficacy.

Without good understanding on the regulatory requirements for medical devices in Taiwan, starting a Manufacturing facility (full or semi finish product) or Importing finished medical devices from overseas manufacturer can be a challenge.

Our trainer Ms Juliana from Taiwan was specially invited to conduct “Understanding Taiwan’s Regulatory Framework for Medical Devices”. This is also the first time such an event is held in Singapore. This event was jointly organized by Singapore Manufacturing Federation and DH RegSys and supported by SGS.

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