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Introduction to Post-Market Surveillance and Vigilance of Medical Devices

This course deals with post-market activities for medical devices. By the end of this course, participants will be equipped to conduct various Post-Market Surveillance activities.

Course Details

The aims and learning outcomes of this course are:

  • To understand the requirements of Post-Market Surveillance.
  • To understand the requirements of vigilance.

Following completion of this course, participants should:

  • Understand a wide variety of post-market activities.
  • Be able to actively participate in the processes of PMS and Vigilance.
  • Have a working knowledge of how to procedurally approach the post-market activities of the regulation.

This is a one-day course in which participants will fully engage with the lecturer through group and individual exercises.  There are plenty of opportunities to ask questions, and the course can be fully tailored to the company’s products and internal structure.  The course is broken down into three modules, taking an in-depth look at post-marketing activities and their interrelatedness.

  1. Introduction to Post-Market Surveillance.
  2. Procedures and methods.
  3. Vigilance.