One of the key factors for ensuring quality of medical technology is the regulatory control of manufacturing, which is supported by a robust Quality Management System for continued compliance during audits. Thus, to maintain product quality after entering the market, a reliable system must properly monitor and regulate these manufacturing activities, which is pivotal to a strategy for successful product design and development.

This course covers the production, quality management systems, and regulatory activities related to quality assurance of medical technology in regulated markets.

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

The Centre of Regulatory Excellence is an accredited provider for Continuing Professional Education (CPE) for Pharmacists and Continuing Medical Education (CME) for Doctors.

Continuing education credits are available for CoRE events through the Singapore Pharmacy Council and the Singapore Medical Council subject to their respective approvals.

Attendees who wish to avail of the credits are required to sign the relevant registration form along with their CPE/CME number on the day of the events.

The attendee’s registration details will be submitted after the event and credited upon receiving respective approvals.