# The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019, Regulation 88: Amendment of regulation 79 (failure to provide information on marketing authorisations to EMA)

Extent: E+W+S+N.I.

In regulation 79 (failure to provide information on marketing authorisations to EMA)—
(a) in paragraph (1), for the first reference to “a marketing authorisation” substitute “a UKMA(NI) or UKMA(UK)”;
(b) in paragraph (2), for the first reference to “a marketing authorisation” substitute “UKMA(NI) or UKMA(UK)”.

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Source: https://www.legislation.gov.uk/uksi/2019/775/regulation/88 (the official version)
Page: https://openlegislation.uk/human-medicines-amendment-etc-eu-exit-regulations-2019/regulation-88
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.