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7.—(1) Subject to regulations 8, 9, 19 and 23, a person who makes an application—
(a)under regulation 4 of the 1994 Regulations for the variation of a United Kingdom marketing authorization;
(b)under section 30 of the Act for the variation of a provision of a product licence, a manufacturer’s licence or a wholesale dealer’s licence; and
(c)under section 39(4) of the Act for the variation of a provision of a clinical trial certificate,
shall pay the fees mentioned in paragraph (2).
(2) The fees referred to in paragraph (1) are—
(a)the fee prescribed in Part III of Schedule 1 in connection with the application; and
(b)in respect of any inspection of a description referred to in paragraph 1 of Schedule 2 made in connection with the application, the fee payable in accordance with paragraphs 2 to 6 of that Schedule.
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