Officers and regulatory representatives of BEHRINGER
OTTONELLO Roberta
ensuring that:
a) the conformity of devices is adequately controlled in accordance with the quality management system under which devices are manufactured before the release of a device;
b) the technical documentation and the EU declaration of conformity are drawn up and updated;
c) the post-market surveillance obligations referred to in Article 10(10) of the MDR are fulfilled;
d) the vigilance reporting obligations referred to in Articles 87 to 91 of the MDR are fulfilled.