2026 GMS5106 Regulation of Digital Health Products

In today's digital world, technologies and software play an increasingly important role in healthcare management -
diagnosis, treatment, patient monitoring and real-world data collection. Software-based medical devices require more streamlined and efficient regulatory oversight due to their higher turnaround times, need for continuous validation and verification, as well as robust software development practices.

Effective governance should account for the dynamic nature of software development, ensuring timely compliance and continuous improvement to maintain safety, quality, and efficacy. Software standards and guidelines published by standards development organisations (eg., ISO, EC) and regulatory agencies/forums are important tools to aid effective
governance allowing timely access for patients.

How the GMS5106 Regulation of Digital Health Products can benefit your career

This course covers essential topics including regulatory frameworks, risk management principles, and post-market surveillance for digital health products.

Due to the limited availability of seats, early registration is strongly recommended.

Click here for a step by step guide on how to register.

Programme

To be advised.

Fees

 

Click here to find out more about the Course Fees.

Continuing Education Credits

CoRE is an accredited provider and continuing education credits are available for pharmacists through the Singapore Pharmacy Council (SPC).

Attendees who wish to avail of these credits are required to sign the relevant registration form along with their CPE number. The attendee’s details will be submitted to SPC after the event and credited upon SPC’s approval.