Post market vigilance is a key regulatory function in the total product life cycle. Continual monitoring and reporting of medical device adverse events is critical in ensuring the marketed devices are free from unacceptable risk.

This course introduces the key activities and roles essential for effective post-market vigilance, including adverse events, field safety correcting action and change management.

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.