Guidelines on the details of the various categories of variations, on the operation of the procedures laid down in Chapters II, II a, III and IV of 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 and on the documentation to be submitted pursuant to those procedure. OJ C 223, 2.8.2 013, 1–79
Accessed on 30th September 2024 at: