DECISION OF THE EEA JOINT COMMITTEE No 7/2023

of 3 February 2023

amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2023/2315]

THE EEA JOINT COMMITTEE,

Having regard to the Agreement on the European Economic Area (“the EEA Agreement”), and in particular Article 98 thereof,

Whereas:

(1) Commission Delegated Regulation (EU) 2022/2239 of 6 September 2022 amending Regulation (EU) No 536/2014 of the European Parliament and of the Council as regards labelling requirements for unauthorised investigational and unauthorised auxiliary medicinal products for human use ( 1 ) is to be incorporated into the EEA Agreement.

(2) Annex II to the EEA Agreement should therefore be amended accordingly,

HAS ADOPTED THIS DECISION:

Article 1

The following indent is added in point 18 (Regulation (EU) No 536/2014 of the European Parliament and of the Council) of Chapter XIII of Annex II to the EEA Agreement:

‘-

32022 R 2239 : Commission Delegated Regulation (EU) 2022/2239 of 6 September 2022 ( OJ L 294, 15.11.2022, p. 5 ).’

Article 2

The text of Delegated Regulation (EU) 2022/2239 in the Icelandic and Norwegian languages, to be published in the EEA Supplement to the Official Journal of the European Union , shall be authentic.

Article 3

This Decision shall enter into force on 4 February 2023, provided that all the notifications under Article 103(1) of the EEA Agreement have been made ( *1 ) .

Article 4

This Decision shall be published in the EEA Section of, and in the EEA Supplement to, the Official Journal of the European Union .

Done at Brussels, 3 February 2023.

For the EEA Joint Committee

The President

Nicolas VON LINGEN

( 1 ) OJ L 294, 15.11.2022, p. 5 .

( *1 ) No constitutional requirements indicated.

ELI: http://data.europa.eu/eli/dec/2023/2315/oj

ISSN 1977-0677 (electronic edition)