# The Medicines (Products for Human Use — Fees) Regulations 1991, Regulation 7: Variations of licences and certificates


Subject to regulations 8, 9, 19 and 23, in connection with an application 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 under section 39(4) for the variation of a clinical trial certificate, there shall be payable by the applicant—
(a) the fee prescribed in Part III of Schedule 1 in connection with that application; and
(b) in respect of any inspection of a description referred to in paragraph 1 of Schedule 2 made in connection with that application, the fee payable in accordance with paragraphs 2 to 5 of that Schedule.

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Source: https://www.legislation.gov.uk/uksi/1991/1474/regulation/7 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-1991/regulation-7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.