![](http://www.interamericancoalition-medtech.org/regulatory-convergence/wp-content/uploads/sites/4/2021/07/who_post_market_en.jpg)
In 2020 the World Health Organization launched the “Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics”.
According to WHO, the document brings out a series of activities to be conducted by manufacturers ” to collect and evaluate experience gained from medical devices that have been placed on the market, and to identify the need to take any action.”
Read the document: