# The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019, Regulation 41: Amendment of regulation 45F (provision of information)


In regulation 45F(1) for sub-paragraph (b) substitute—
“(b) either—
(i) the UK marketing authorisation holder; or
(ii) where applicable, the holder of the licence or authorisation granted by an appropriate authority responsible for the licensing of medicinal products in an approved country for import;”.

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Source: https://www.legislation.gov.uk/ukdsi/2019/9780111179185/regulation/41 (the official version)
Page: https://openlegislation.uk/draft-human-medicines-amendment-etc-eu-exit-regulations-2019/regulation-41
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.