The Commission shall, by the last day of the third year following the granting of the first Union compulsory licence in accordance with Article 7, present to the European Parliament, the Council and the European Economic and Social Committee an evaluation report on the application of this Regulation.
The Commission shall regularly, and for the first time by 31 December 2027, assess whether the list in the Annex is up to date, including, in particular, in relation to semiconductors for medical equipment. It may, where appropriate, submit proposals to amend the Annex.
Every five years from 19 January 2026, the Commission shall report on the assessments carried out pursuant to the second paragraph to the European Parliament and the Council.
Text as published in the Official Journal, reproduced verbatim (including any typographical quirks of the source). For the authentic version, see EUR-Lex.
