June 12, 2018

HSA proceeds in the next step of revising several existing guidance documents for medical device registration after conducting an industry briefing last February. HSA held a public consultation to get feedbacks from concerned stakeholders before they finalized the proposed changes. The following were the schedule for consulting the guidance revisions. 

Outcomes of these consultation sessions have been consolidated and new revisions to the existing guidance documents and issuance of new guidance documents are to be carried out in stages, after this. Qualtech will bring to you all the latest regulatory updates in Singapore, following this major reformation, in future newsletter updates.