This article is part of the network’s archive of useful research information. This article is closed to new comments due to inactivity. We welcome new content which can be done by submitting an article for review or take part in discussions in an open topic or submit a blog post to take your discussions online.
This review presents the strategies for postmarket surveillance of medical devices in the United States, European Union, Japan and China and present suggestions for best practice in post market surveillance.
To read the full article, published in PLoS Medicine, click on the following link: http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001519