1979 No. 382
The Medicines (Chloroform Prohibition) Order 1979
Made
Laid before Parliament
Coming into Operation
The Secretaries of State respectively concerned with health in England, in Wales and in Scotland and the Department of Health and Social Services for Northern Ireland, acting jointly, in exercise of powers conferred by section 62 of the Medicines Act 1968 and now vested in them1 and of all other powers enabling them in that behalf, it appearing to them to be necessary in the interests of safety to make the following Order, after consulting such organisations as appear to them to be representative of interests likely to be substantially affected by the Order, and after consulting and taking into account the advice of the Committee on Safety of Medicines2, and after taking into account the report of the Medicines Commission made under section 62(5) of that Act, hereby make the following Order:—
Citation, commencement and interpretation1
1
This Order, which may be cited as the Medicines (Chloroform Prohibition) Order 1979, shall come into operation on 28th March 1980.
2
In this Order, “the Act” means the Medicines Act 1968.
3
In this Order a reference to a numbered Article is a reference to the Article of this Order bearing that number and a reference in a paragraph of an Article of this Order to a lettered sub-paragraph is a reference to the sub-paragraph of that paragraph bearing that letter.
Prohibition of sale or supply of chloroform2
Subject to the exceptions specified in Article 3 the sale or supply of any medicinal product consisting of or containing chloroform, not being a veterinary drug, is hereby prohibited.
Exceptions3
1
The prohibition imposed by Article 2 shall be subject to the exception that the sale or supply of any medicinal product described in that Article shall not by virtue of that Article be prohibited where such sale or supply is—
a
by a doctor or dentist to a patient of his and the medicinal product has been specially prepared by that doctor or dentist for administration to that particular patient, or
b
by a doctor or dentist who has specially prepared the medicinal product at the request of another doctor or dentist for administration to a particular patient of that other doctor or dentist, or
c
from a registered pharmacy or a hospital or by a doctor or dentist and the medicinal product has been specially prepared, in accordance with a prescription given by a doctor or dentist for a particular patient of his—
i
in a registered pharmacy, or
ii
in a hospital, or
iii
by a doctor or dentist, or
iv
by a person to whom there applies an exemption from the restrictions imposed by section 8(2) of the Act (restrictions as to manufacture or assembly) by virtue of Article 3 of the Medicines (Exemption from Licences) (Special and Transitional Cases) Order 1971.
2
The prohibition imposed by Article 2 shall be subject to the additional exception that the sale or supply of any such medicinal product shall not be prohibited by virtue of that Article where such sale or supply is—
a
to a hospital or to a doctor or to a dentist for either or both of the following purposes, namely—
i
solely for use by administration to human beings for the purpose of inducing anaesthesia, or
ii
solely for use as an ingredient in the preparation of a substance or article to be administered to human beings for the purpose of inducing anaesthesia, or
b
to a person who buys or obtains it for the purpose of selling or supplying it to a hospital or to a doctor or to a dentist for either or both of the purposes described in sub-paragraph (a).
3
The prohibition imposed by Article 2 shall be subject to the additional exceptions that the sale or supply or any such medicinal product shall not by virtue of that Article be prohibited in any one or more of the following circumstances, namely—
a
where such product contains chloroform in a proportion of not more than 0.5 per cent calculated in terms of weight in weight (w/w) or volume in volume (v/v) as appropriate, or
b
where such product is solely for use in dental surgery, or
c
without prejudice to sub-paragraph (b) where such product is for sale or supply solely for use by being applied to the external surface of the body.
4
The prohibition imposed by Article 2 shall be subject to the additional exception that the sale or supply of any such medicinal product shall not by virtue of that Article be prohibited where the said sale or supply involves, or is for the purpose of, exporting the said medicinal product.
5
The prohibition imposed by Article 2 shall be subject to the additional exception that the sale or supply of any such medicinal product shall not by virtue of that Article be prohibited where the medicinal product is for use as an ingredient in the preparation of any substance or article—
a
in a registered pharmacy, or
b
in a hospital, or
c
by a doctor, or
d
by a dentist.
6
For the purposes of this Article the external surface of the body shall not include the mouth or any part of the mouth (including teeth) or the mucous membranes.
Transitional provisions4
The prohibition imposed by Article 2 shall not operate during a period of one year from the date of the coming into operation of this Order in the case of medicinal products consisting of or containing chloroform which have, before that date, been sold or supplied for retail sale or for supply in circumstances corresponding to retail sale.
Sealed with the official seal of the Department of Health and Social Services for Northern Ireland this 27th day of March 1979.