http://www.legislation.gov.uk/eur/2008/1234/annex/IV/division/5
Commission Regulation (EC) No 1234/2008 of 24 November 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)
Commission Regulation (EC) No 1234/2008
Commission Regulation (EC) No 1234/2008 of 24 November 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)
2020-12-13
King's Printer of Acts of Parliament
https://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02008R1234-20130804
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2013-08-04
Commission Regulation (EC) No 1234/2008 of 24 November 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)
Regulation
The Veterinary Medicines (Amendment etc.) Regulations 2024
reg. 209
reg. 1(1)
Commission Regulation (EC) No 1234/2008 of 24 November 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)
Regulation
The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019
Sch. 9
para. 1(p)
reg. 1
ANNEX IVElements to be submitted
5.
In the case of variations to centralised marketing authorisations, the relevant fee provided for in Council Regulation (EC) No 297/959.