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2024 GMS5114 Post-Market for Medical Technologies

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.

 
   


Date and Time


06 May 2024 @ 08:30 - 10 May 2024 @ 17:30

Speaker


 

Venue


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