Due to two new regulations for medical devices that are expected to enter into force in the second quarter of 2017, two information days for economic operators are planned:
On 31 May , an information day on the “Medical Devices Regulation” (MDR) is organized for manufacturers, authorized representatives, importers and distributors of medical devices.
On June 13, an information day on the “Regulation on medical devices for in vitro diagnostics” (IVDR) will be organized at the Medical Products Agency in Uppsala. The information day is aimed at manufacturers, authorized representatives, importers and distributors of in vitro diagnostic medical devices.
**More information and program content will be published shortly. It will also be possible to register for the event relevant to the products the company manufactures, imports, distributes or is an authorized representative for.