Giorgio Calesella organized an in house seminar entitled: "The new EU Regulation on medical devices 2017/745 - (MDR): possible impact on the Procurement Code". The objective of the seminar was to gather thoughts on new legislations (new European regulation on medical devices and Procurement code) that strongly impact orders by government entities and the supply of medical devices, and dedicate time to focus on: Product specifications and description of product specifications in tender specifications; Special law on procurement and causes of exclusion for technical reasons; The person responsible for compliance with regulations (art. 15).