a)The conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released
b)The Technical documentation and the EU declaration of conformity are drawn up and kept up to date
c)Declaration on General Safety and Performance for devices in clinical investigation is issued
d)Post-Market surveillance obligations are complied with in accordance with Article 10 (10) of the MDR 2017/745