The new European regulation 2017/745 about medical devices, entered into force on 25 may 2017 and repealing the previous directive 93/42/EEC, introduces major changes in the legal framework governing the placing on the European market for medical devices.
The seminar to be held at the headquarters of the laboratory CATAS Brianza in Lissone (MB) Thursday, 20 September at 14.00 aims to frame the new legislative context in which are medical devices and the main changes introduced by the new regulation concerning verification of conformity of products and the obligations of operators.
The event attended by the dott. Andrea Giavon, Director of CATAS, Alberto Gelosa, responsible for CATAS Brianza and the dott. Roberto Passini, Director of Sicom testing, Lab testing and certification of electrical products, electronic and radio, dealing with the regulatory framework in the event that the products are integrated with control devices or motorized movements.
The seminar is free and you can subscribe to the following link.