The Human Medicines (Amendment) (No. 2) Regulations 2014
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Change 1
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— is granted by the licensing authority in compliance with the rules of European Union Law relating to parallel imports; and authorises the holder to place on the market a medicinal product imported into the United Kingdom from another EEA State; .
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— is granted by the licensing authority in compliance with the rules of European Union Law relating to parallel imports; and authorises the holder to place on the market a medicinal product imported into the United Kingdom from another EEA State; .
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