Paragraph 70
In regulation 1(2) of the Medical Devices (Consultation Requirements) (Fees) Regulations 1995 M1—
(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 ”.