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)
- Draft of Medicinal Products (Control of Placing on the Market) Regulations 2005 (PDF)
- Explanatory document
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)
- Draft of Medicinal Products (Control of Advertising) Regulations 2005 (PDF)
- Draft of Medicinal Products (Control of Manufacture) Regulations 2005 (PDF)
- Draft of Medicinal Products (Control of Wholesale Distribution) Regulations 2005 (PDF)
Please note that the date of acceptance of submissions on these draft Regulations has now passed.
