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Statutory Instrument

The Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1995

Citation
S.I. 1995/309
As at
Sections
3
Section 1Citation, commencement and interpretation

(1) This Order may be cited as the Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1995 and shall come into force on 20th February 1995.

(2) In this Order—

“certificate of registration” means a certificate for the purposes of the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994 ;

“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.

Section 2Advisory Board on the Registration of Homoeopathic Products

(1) The Advisory Board on the Registration of Homoeopathic Products, provision for the establishment of which was made by article 2 of the Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1994 , is a committee established for the purpose of giving advice with respect to the safety and quality of—

(a) any homoeopathic medicinal product in respect of which the conditions set out in paragraph (2) below are met; and

(b) any homoeopathic medicinal product which satisfies the conditions set out in Article 7 of Council Directive 92/74/EEC ,

and to which any provision of the Medicines Act 1968 is applicable.

(2) The conditions referred to in paragraph (1)(a) above are that:

(a) the product is one to which Article 2(1) of Council Directive 92/73/EEC applies;

(b) the product is for oral or external administration;

(c) no specific therapeutic indication appears on the labelling of the product or in any information relating thereto;

(d) the product is one in respect of which—

(i) an application for a certificate of registration has been made in accordance with regulation 4(1) of the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994, or

(ii) an application for the renewal of such a certificate has been made in accordance with regulation 8(3) of those Regulations, or

(iii) the licensing authority proposes to suspend or revoke the certificate of registration.

Section 3Revocation

The Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1994 is hereby revoked.

3 sections

Cite this legislation

The Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1995 (legislation.gov.uk, OGL v3.0). Retrieved via LawPlayer, https://lawplayer.com/uk/act/uksi-1995-309

Contains public sector information licensed under the Open Government Licence v3.0.

OGL-3

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