Post Market Surveillance: an Introduction
Course Description:
This course explains what post-market surveillance is and what potential activities should be included in the post-market surveillance plan for a given product.
Watch the Course Trailer:
Learning Objectives:
Upon successfully completing this course, learners will be able to:
- Plan post-market surveillance activities in relation to the risk management and continuous improvement processes
Who Should Enroll:
Professionals new to the medical device industry, including inventors, managers, CEOs, or professionals wanting an overview of the global lifecycle of medical devices are all welcome to participate in this course.
Prerequisite Knowledge/Requirements:
The following material is required:
- Knowledge of all aspects of the medical device lifecycle, including risk management, design, and validation
- The Lifecycle of Medical Devices from Idea to Market (ID 159)
- Creating Value in Healthcare (ID 175)
- What is considered a Medical Device? (ID 161)
- The Main Concepts for Safe and Performing Devices (ID 163)
- Clinical Evaluation of Medical Devices: An Introduction (ID 165)
- Business Plan Essentials for Medical Products (ID 177)