Is the EU underplaying the device interference problem?
This article was originally published in Clinica
Executive Summary
Is there enough regulation in the EU to avoid the potentially fatal outcomes for patients that could occur when electromedical or electronic medical devices interfere with each other or with other equipment? And are manufacturers taking enough care to ensure that they are not exposing themselves to the litigious consequences of being negligent in ensuring that such devices operate properly in the environment for which they are intended?