Statutory Instruments

Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 2002

The Regulations are also intended to give effect, on an on-going basis, to the various classification for the supply of medicinal products for human use that arise in connection with the authorisation of such products, in the context of Directive 2001/83/EC of the European Parliament and of the Council relating to medicinal products for human use and having particular regard to Title VI of this Directive which relates to the classification of medicinal products

The Regulations also incorporate amendments to provide exemptions so as to enable certain homeopathic medicinal products to be supplied without a medical prescription and to enable the supply of certain prescription-only herbal medicinal products to be supplied in certain defined circumstances

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