Draft Commission Delegated Regulation amending Regulation (EC) No 1272/2008 as regards the harmonised classification and labelling of certain substances; (7 page(s), in English), (15 page(s), in English)

Draft amendments to the Rules for marketing authorization and assessment of medicinal products for human use; (24 page(s), in Russian)

International harmonisation of ingredient names (IHIN) – Dual labelling transition to sole medicine ingredient names; (21 page(s), in English)