Statutory Instruments

The Medicinal Products (Prescription and Control of Supply) Regulations 2003

The main purpose of these Regulations is to consolidate and to update the controls applicable to the prescription and supply of medicinal products to the public in accordance with the requirements of E.U. Directive 2001/83/EC of 6th November 2001 insofar as that Directive relates to the classification for the supply of medicinal products for human use (OJ No L311, 28.11.2001, p67). The Regulations also set out the classification for supply of medicinal products to the public as required by that Directive

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