This training covers post-sales surveillance activities required to monitor the performance and safety of medical devices after they enter the market. In line with Meddev 2.12.1 and Meddev 2.12.2 guidelines, detailed information is provided on aftermarket surveillance plans, monitoring methods and reporting processes.

Participants learn how to take proactive measures to minimize potential risks by continuously monitoring the performance of their devices. This training helps manufacturers to develop an aftermarket surveillance program that complies with regulatory requirements.