# Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 2005, Paragraph 4


(1) The Medicines (Advisory Board on the Registration of Homoeopathic Products) Order 1995 is amended as follows.
(2) In regulation 1 (citation, commencement and interpretation), in paragraph (2), in the definition of “homoeopathic medicinal product” omit “products,” and “or compositions”.
(3) In regulation 2 (Advisory Board on the Registration of Homoeopathic Products)—
(a) omit paragraph (1)(b);
(b) in paragraph (2)(a), after “human use” insert “as amended by Directive 2002/98/EC of the European Parliament and of the Council setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components, Commission Directive 2003/63/EC amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, Directive 2004/24/EC of the European Parliament and of the Council amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use and Directive 2004/27/EC of the European Parliament and of the Council amending Directive 2001/83/EC on the Community code relating to medicinal products for human use”; and
(c) in paragraph (2)(d)—
(i) in head (ii) for “8(3)” substitute “8(2)”, and
(ii) in head (iii) for “suspend or revoke” substitute “suspend, vary or revoke”.

---
Source: https://www.legislation.gov.uk/uksi/2005/2753/schedule/paragraph/4 (the official version)
Page: https://openlegislation.uk/medicines-homoeopathic-medicinal-products-for-human-use-amendment-regulations-2005/schedule/paragraph-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.