European manufacturers must act to stop misuse of devices or face new regulation
This article was originally published in Clinica
Executive Summary
The medical devices industry needs to draw up a code of practice urgently to prove it is doing everything in its power to limit the misuse of products by users. If manufacturers delay in addressing this issue, they risk prosecution and the industry as a whole will be vulnerable to further regulatory controls, according to medical device expert Dario Pirovano.