Brussels, 28/02/2003 (Agence Europe) - The Council's working group has finished assessing the draft regulation on the European Medicines Agency, but the European Commission is finding it hard to finalised its amended draft directive on the authorisation of medicines for human use. First announced for the end of January, then for February, it is unlikely to be completed before the end of March. When it voted on the regulation and the two directives (the other one concerning veterinary...