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The Medicines (Applications for Product Licences and Clinical Trial and Animal Test Certificates) Amendment Regulations 1977

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Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol). This item of legislation is currently only available in its original format. The electronic version of this UK Statutory Instrument has been contributed by Westlaw and is taken from the printed publication. Read more

Amendments of Schedule 1 to the principal regulations

2.—(1) After paragraph 27 of Part I of Schedule 1 to the principal regulations (particulars required on applications) there shall be inserted the following paragraphs—

“28.  A specimen or mock-up of the labelled container and package in which the medicinal product is to be sold or supplied and a specimen or mock-up of any leaflet relating to the medicinal product which is to be supplied with the product by being enclosed in containers or packages of the product.

29.  Where manufacturing or assembling operations relating to the medicinal product are to be carried out in a place other than in the United Kingdom, documentary evidence that every person taking part in the manufacture or assembly in the course of a business carried on by him is authorised to carry out such operations by the appropriate authority of the country in which such operations are to be carried out.

30.  Where an authorisation to sell or supply the medicinal product or to place the product on the market in another country has been obtained, a copy of such authorisation.”.

(2) After paragraph 28 of Part II of Schedule 1 to the principal regulations there shall be inserted the following paragraphs—

“29.  A specimen or mock-up of the labelled container and package in which the medicinal product is to be sold or supplied and a specimen or mock-up of any leaflet relating to the medicinal product which is to be supplied with the product by being enclosed in containers or packages of the product.

30.  Where manufacturing or assembling operations relating to the medicinal product are to be carried out in a place other than in the United Kingdom, documentary evidence that every person taking part in the manufacture or assembly in the course of a business carried on by him is authorised to carry out such operations by the appropriate authority of the country in which such operations are to be carried out.

31.  Where an authorisation to sell or supply the medicinal product or to place on the product on the market in another country has been obtained, a copy of such authorisation.”.

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