This section has no associated Explanatory Memorandum
70. In regulation 1(2) of the Medical Devices (Consultation Requirements) (Fees) Regulations 1995 M1—U.K.
(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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