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Regulatory Impact Assessment on the Proposed Regulation of Medical Devices in Hong Kong   The Government has commissioned ERM-Hong Kong Limited (ERM) to conduct a Regulatory Impact Assessment (RIA) study on the proposed regulation of medical devices. The aim of the RIA study is to identify and assess different options and impacts of the proposed regulation on the stakeholders, and to recommend possible options. Various stakeholders have been invited to reflect their views by participating in focus group discussion or filling in and returning a questionnaire. If you want to get more information about the RIA study, please contact ERM's Kalvin Lai at 2271 3161 or Elaine Chan at 2271 3192.

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Last revision date: 30 August 2007