European Commission's John Dalli says no need for device pre-market approval
This article was originally published in SRA
Executive Summary
John Dalli, the European commissioner in charge of the department responsible for medical device regulation, gave an impassioned speech last night at the European Parliament in which he argued against the need for a system of pre-market approval for medical devices and championed the industry’s need to innovate and patients’ needs to have access to innovative products.