# The Human Medicines Regulations 2012, Paragraph 70


In regulation 1(2) of the Medical Devices (Consultation Requirements) (Fees) Regulations 1995 —
(a) in the definition “authorised medicinal product”—
(i) in sub-paragraph (b) before “under” insert “ the Human Medicines Regulations 2012 or ”, and
(ii) in sub-paragraph (c) for “those” substitute “ the latter ”; and
(b) in the definition “product licence of right” for “section 25(4) of that Act” substitute “ paragraph 3(2) of Schedule 32 to the Human Medicines Regulations 2012 ”.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/34/paragraph/70 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-34/paragraph-70
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.