# The Human Medicines (Amendment) (No. 2) Regulations 2014, Regulation 6: Amendment of regulation 50


(1) Regulation 50 (material to accompany applications for UK marketing authorisations) is amended as follows.
(2) After paragraph (1) insert—
“(1A) An applicant for the grant of a parallel import licence for a relevant medicinal product must provide the material specified in Schedule 8A in relation to the product.”
(3) In paragraph (4) after “application” insert “for a UK marketing authorisation”.
(4) In paragraph (5) after “regulation” insert “for the purposes of a UK marketing authorisation”.
(5) In paragraph (6) for “This” substitute “Unless the application is for a parallel import licence this”.

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Source: https://www.legislation.gov.uk/uksi/2014/1878/regulation/6 (the official version)
Page: https://openlegislation.uk/human-medicines-amendment-no-2-regulations-2014/regulation-6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.