Getting your device onto the Singapore market

22 Aug 2019
21 May 2018 | 11am
CeLS Auditorium

Getting your device onto the Singapore market

In Singapore, medical devices are regulated by the Health Sciences Authority to safeguard public health and safety. All medical devices, will need to be registered with HSA before supply unless they are for clinical trials, are custom made, and/or are Class A non-sterile devices.
This talk provides an introduction to the product registration process by HSA, covering the documentation requirements for the various device risk classifications.