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Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 2005

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This is the original version (as it was originally made). This item of legislation is currently only available in its original format.

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1.—(1) Section 7 of the Act (general provisions as to dealing with medicinal products) is amended as follows.

(2) Subsections (2A) and (2B)(1) are repealed.

(3) After subsection 3A(2) insert the following subsection—

(3B) The restrictions imposed by subsections (2) and (3) of this section shall not apply where the medicinal product concerned is a homoeopathic medicinal product to which the 2001 Directive applies and which fulfils the conditions laid down in Article 14(1) of that Directive..

(4) In subsection (7)(3)—

(a)the definition of “certificate of registration” is repealed; and

(b)in the definition of “homoeopathic medicinal product”, the words “products,” and “or compositions” are repealed.

(1)

Subsections (2A) and (2B) were inserted by regulation 3(2) of S.I. 1994/276.

(2)

Subsection (3A) was inserted by regulation 54 of S.I. 2004/1031.

(3)

Subsection (7) was substituted by regulation 2(3) of S.I. 1983/1724 and amended by regulation 2(5) of S.I. 1992/604 and regulation 3(4) of S.I. 1994/276.

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