The European Commission proposes an extension of the transitional period for the re-certification of medical devices
On 06 January 2023, the European Commission proposed an extension of the transitional period for the re-certification of medical devices in order to reduce any risk of shortages. There are at present more than 500,000 types of medical devices on the EU market, ranging from simple contact lenses and plasters to pacemakers and hip replacements, […]
