HSA Guidance Documents — by Topic
Finding HSA guidance
All current HSA guidance documents for medical devices are published on the HSA website:
hsa.gov.sg/medical-devices/guidance-documents
Guidance documents are updated periodically. Always use the current version from the HSA website — do not rely on downloaded copies that may be outdated.
Guidance by topic area
Registration and classification
- Quick Guide to Medical Device Registration and Licensing (April 2026)
- Risk classification guidance documents
- Registration guides by class and route (see Registration Guides)
Device grouping
- Guidance on grouping types (Family, System, Group, Single)
- Dental Grouping Terms (DGT)
- IVD grouping guidance
Clinical evidence
- Clinical evidence requirements for medical device registration
- Guidance on clinical investigations
Quality management systems
- QMS requirements for dealer's licences
- GDP guidance for importers and wholesalers
Post-market
- Adverse event reporting guidance
- FSCA reporting guidance
- Change notification guidance
Digital health and SaMD
- Digital health guidance documents (see HSA Digital Health)
Labelling and advertising
- Labelling guidance for medical devices
- Advertising guidelines for medical devices
Specific device types
- Custom-made medical devices
- Guidance for specific device categories as published by HSA
Official sources
Remove the date from 'Quick Guide to Medical Device Registration and Licensing (April 2026)' or replace with 'Quick Guide to Medical Device Registration and Licensing' and add a note: 'Always check the HSA website for the current version, as publication dates may change.'