Consultation on 2001 Review of Pharmaceutical Legislation

Implementation of Directive 2001/83/EC (as amended by Directives 2002/98/EC, 2004/24/EC and 2004/27/EC) relating to the placing on the market of medicinal products for human use

This implementation embraces Titles III (placing on the market), V (labelling and packaging), VI (classification of medicinal products) and IX (pharmacovigilance) of Directive 2001/83/EC)

Please note that the date of acceptance of submissions on these draft Regulations has now passed.

Implementation of Titles IV (on manufacture), VII (on wholesaling), VIII and VIIIa (on advertising) of Directive 2003/2001/EC (as amended by Directive 2004/27/EC)

Please note that the date of acceptance of submissions on these draft Regulations has now passed.