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(1) This Order may be cited as the Medicines (Aristolochia) (Emergency Prohibition) Order 1999, shall come into force on 28th July 1999 and shall continue in force until the end of 27th October 1999, when it shall expire.
(2) In this Order, “the Act” means the Medicines Act 1968.
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(1) Subject to paragraphs (2), (3) and (4) below, the sale, supply, and importation of any medicinal products consisting of or containing a plant belonging to a species of the genus Aristolochia, or any extracts from such a plant, is prohibited.
(2) The prohibition imposed by paragraph (1) above shall not apply to the sale, supply or importation of the medicinal products referred to where the sale or supply is to, or, in the case of importation, the importation is made by or on behalf of, any of the following persons—
(a) a food analyst or food examiner within the meaning of section 30 of the Food Safety Act 1990;
(b) a food analyst or food examiner within the meaning of Article 30 or 31 of the Food Safety (Northern Ireland) Order 1991;
(c) an authorised officer within the meaning of section 5(6) of the Food Safety Act 1990, or Article 2(2) of the Food Safety (Northern Ireland) Order 1991;
(d) a person duly authorised by an enforcement authority under sections 111 and 112 of the Act;
(e) a sampling officer within the meaning of Schedule 3 to the Act.
(3) The prohibition on importation imposed by paragraph (1) above shall not apply to the importation of the medicinal products referred to—
(a) from a member State of the European Community, or
(b) if the products originated in an EEA State within the meaning of Article 9 of, and Protocol 4 to, the Agreement on the European Economic Area signed at Oporto on 2nd May 1992, as adjusted by the Protocol signed at Brussels on 17th March 1993, from an EEA State other than a member State.
(4) The prohibition imposed by paragraph (1) above shall not apply to the sale, supply or importation of the medicinal products referred to where the products are the subject of a product licence, a marketing authorization within the meaning of regulation 1(4)(a) of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 or a certificate of registration within the meaning of regulation 1(2) of the Medicines (Homoeopathic Products for Human Use) Regulations 1994.
Signed by authority of the Secretary of State for Health
Hayman
Parliamentary Under Secretary of State
Department of Health
22nd July 1999Signed by authority of the Secretary of State for Wales
Jon Owen Jones
Parliamentary Under Secretary of State Welsh Office
23rd July 1999Calum MacDonald
Parliamentary Under Secretary of State Scottish Office
23rd July 1999Sealed with the Official Seal of the Department of Health and Social Services for Northern Ireland on
D. C. Gowdy
Permanent Secretary
23rd July 1999