# The Human Medicines (Amendment) (No. 2) Regulations 2014, Regulation 3: Amendment of regulation 48


In regulation 48(2) (definitions in relation to the Part on marketing authorisations), after the definition of “generic medicinal product” insert—
““parallel import licence” means a licence that—
(a) is granted by the licensing authority in compliance with the rules of European Union Law relating to parallel imports; and
(b) authorises the holder to place on the market a medicinal product imported into the United Kingdom from another EEA State;”.

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Source: https://www.legislation.gov.uk/uksi/2014/1878/regulation/3 (the official version)
Page: https://openlegislation.uk/human-medicines-amendment-no-2-regulations-2014/regulation-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.