correcting certain language versions of Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use

This procedure involves correcting errors in the language versions of an existing regulation. The regulation concerns the rules for changing the terms of marketing authorisations for human medicines.

This affects pharmaceutical companies and regulatory bodies involved in authorising and managing medicinal products. It ensures consistency and accuracy in the legal framework governing these authorisations.