Check the conformity of the devices in accordance with the quality management system under which the devices are manufactured, before a device is released. Keep the technical documentation and the EU declaration of conformity up-to-date. PMS obligations in accordance with Article 10(10). Ensure that he reporting obligations referred to in Articles 87 to 91 are fulfilled and in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.