Introduction to Post-Market Surveillance and Vigilance of Medical Devices

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.
• All participants should have a working knowledge of how to procedurally approach the post-market activities of the regulation.

This three module course is held live in an online lecture theatre and delivered with a PowerPoint presentation.  All participants will fully engage with the lecturer through both group and individual exercises and direct participation throughout the course.  There are exercises included in order to ensure the course contents are fully understood and the opportunity is always available for participants to ask questions.

This course takes an in-depth look at post-marketing activities and how they are interrelated. It is broken down into 3 modules.

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