# The Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994, Paragraph 4


In the Medicines (Manufacturer’s Undertakings for Imported Products) Regulations 1977 for paragraph (1) of regulation 2 there shall be substituted the following paragraph—
“(1) In these Regulations, unless the context otherwise requires—
(a) “medicinal product” includes a relevant medicinal product within the meaning of the Medicines for Human Use (Marketing Authorizations Etc.) Regulations 1994 and, where a product licence relates to any substance or article which is not a medicinal product, the substance or article to which the licence relates or is intended to relate;
(b) “product licence” includes a marketing authorization within the meaning of the Medicines for Human Use (Marketing Authorizations Etc.) Regulations 1994; and
(c) other expressions have the same meanings as in the Medicines Act 1968.”.

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Source: https://www.legislation.gov.uk/uksi/1994/3144/schedule/7/paragraph/4 (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-marketing-authorisations-etc-regulations-1994/schedule-7/paragraph-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.