# The Medicines (Products for Human Use — Fees) Regulations 1991, Regulation 4: Applications for licences and certificates


Subject to regulations 5, 19 and 23, in connection with an application for a product licence, a manufacturer’s licence, a wholesale dealer’s licence or a clinical trial certificate, there shall be payable by the applicant—
(a) the fee prescribed in Part II of Schedule 1 in connection with that application; and
(b) in respect of any inspection of a description falling within 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/4 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-1991/regulation-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.