# Commission Regulation (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Text with EEA relevance), Article 2: Transitional arrangements

Extent: E+W+S+N.I.

From 2 November 2012, the following changes shall apply:
(a)in Article 23(1) of Regulation (EC) No 1234/2008, the reference to ‘Chapters II and III’ is replaced by ‘Chapter II’;
(b)in Article 23(1) of Regulation (EC) No 1234/2008, subparagraph (a) is deleted.

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Source: https://www.legislation.gov.uk/eur/2012/712/article/2 (the official version)
Page: https://openlegislation.uk/eu-regulation-2012-712/article-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.