Commission Regulation (EC) No 1234/2008Dangos y teitl llawn

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)

2.A description of all the variations submitted, including:U.K.

(a)

in the case of minor variations of type IA, the date of implementation for each variation described;

(b)

in the case of minor variations of type IA which do not require immediate notification, a description of all minor variations of type IA made in the last 12 months to the terms of the concerned marketing authorisation(s) and which have not been already notified.