Newly issued monitoring and certification procedures, designed to ensure full compliance and traceability of medical devices were agreed by Parliament on Wednesday April 2nd 2014.
The European Parliament’s news release says its amendments would strengthen the procedure for placing new medical devices on the market so as to ensure that unsafe products or devices that have undergone insufficient controlled trials on patients can no longer be used on or in them. Read more here.
Last modified: Mon, 07 Apr 2014 09:34:55 BST