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2025 GMS5114 Post-Market in 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.

How the GMS5114 Post-Market in Medical Technologies can benefit your career

This course will introduce you to the key activities and roles critical for effective post-market vigilance. You will gain insights into managing adverse events, implementing field safety corrective actions, and navigating change management processes.

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

v2 Flyer_2025 GMS5114 Post-Market for Medical Technologies

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

  


Date and Time


21 Apr 2025 @ 08:30 - 25 Apr 2025 @ 17:30

Speaker


 

Venue


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