Register Class D medical device with a registrable drug in a secondary role via full route
Follow this guide to find out what is needed to complete the full registration for Class D devices with a registrable drug in a secondary role.
Eligibility
You must register your Class D medical device with a registrable drug in a secondary role via the full evaluation route if it has not previously been approved by any of our independent reference regulatory agencies, and the chemical or biological component has not been evaluated and approved by a competent drug regulatory agency as defined by the World Health Organisation (WHO).
Submission requirements
You need to submit the documents in English.
ASEAN Common Submission Dossier Template (CSDT)
Executive summary
Device description
Detailed information of design verification and validation documents:
Full reports of preclinical studies e.g. physical test data, biocompatibility studies, animal studies and software verification and validation studies
Sterilisation validation (if applicable)
Shelf-life studies and projected useful life
Clinical Evaluation Report, including publications and full reports of the studies referenced
Proposed device labelling
Risk analysis
Name and address of the manufacturing and sterilisation sites
Proof of at least one Quality Management System below:
ISO 13485
MDSAP
Conformity to US FDA Quality System Regulations
Japan MHLW Ordinance 169
Manufacturing process - flow chart
Additional documents
Fees and turn-around-time
Refer to medical device fees and turn-around-time for more information.
How to register
You will need to register your medical device through the Singapore Health Product Access and Regulatory E-System (SHARE).
You will need the following in order to access SHARE:
If you encounter technical issues with SHARE (e.g. unable to upload documents), please e-mail HSA SHARE Support with the screenshot of the error message including the address bar and system time for assistance.
Full list of registration guides
If you have a device of another risk class or wish to understand other available registration routes, you may access the full list of registration guides.
