Textul licitației

iological medical equipment and will set up up-to-date criteria for acceptability of this equipment, considering developments in technology, standards and requirements that occurred since the publication of RP 162. The contractor must propose criteria for acceptability that are achievable throughout the EU Member States and provide advice on their implementation and verification in practice. The revised document will rely, to the extent possible, on the methodology for defining and applying criteria for acceptability of equipment established in section 1 of RP 162. Any change of the proposed methodology shall be substantiated and approved by DG ENER before progressing with Task 2 of the study as described in the tender specifications. The contractor will develop criteria for acceptability of equipment that came on the market after 2010 or was too new to be addressed in RP 162. This shoul