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1. (1) This Order may be cited as the Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1994 and shall come into force on 14th February 1994.
(2) In this Order—
“the Act” means the Medicines Act 1968;
“certificate of registration” means a certificate granted under the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994(1);
“homoeopathic medicinal product” means a medicinal product (which may contain a number of principles) prepared from products, substances or compositions called homoeopathic stocks in accordance with a homoeopathic manufacturing procedure described by the European Pharmacopoeia or, in the absence thereof, by any pharmacopoeia used officially in a member State.