Advertisement, post-market surveillance and safety monitoring
Find out the requirements related to advertisement, post-market surveillance and safety monitoring.
Last updated 23 April 2026
Adverse events reporting of medical devices
All companies dealing in medical devices including importers, manufacturers, suppliers and registrants are required to report adverse events of their products.
Advertisements and promotions of medical devices
It is the responsibility of the advertiser to ensure compliance with legislation and guidelines for advertisements and promotions of medical devices.
Field Safety Corrective Action
Understand the requirements when implementing a Field Safety Corrective Action (FSCA) for medical devices supplied in Singapore.
