Busi­ness Brunch – MDR: Focus on dis­tri­bu­tors and importers

Busi­ness Brunch with Miri­am Schuh & Saskia Witt­brodt on 30 Novem­ber 2018 in Düsseldorf

The much dis­cus­sed Euro­pean regu­la­ti­ons for the medi­cal devices indus­try have been in force now for over a year. As from May 2020 and 2022 respec­tively, the MDR and the IVDR will be appli­ca­ble to the manu­fac­tu­re, pla­cing on the mar­ket and moni­to­ring of medi­cal devices.

For importers and dis­tri­bu­tors in par­ti­cu­lar, the regu­la­ti­ons bring new sta­tu­to­ry obli­ga­ti­ons. At our busi­ness brunch we will be dis­cus­sing the new­ly defi­ned requi­re­ments and pro­vi­ding infor­ma­ti­on about what it is that importers and dis­tri­bu­tors defi­ni­te­ly need to pay heed to in view of the appli­ca­ble regu­la­ti­ons when desig­ning their con­tracts with manufacturers.

Event­lo­ca­ti­on

Agen­da

Fol­der