# The Medicines (Products for Human Use) (Fees) Regulations 2012, Paragraph 9: Inspection fees in connection with applications


In connection with an application for a marketing authorization, traditional herbal registration, manufacturer’s licence or manufacturing authorisation, the fee payable in respect of an inspection at any site other than one named as a possible site for manufacture of a medicinal product by three or more applicants shall, if the applicant so requests in writing, be payable as to 50% within the period of 14 days referred to in regulation 45(1)(b) and as to 50% within 12 months after that date.

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Source: https://www.legislation.gov.uk/nisr/2012/134/schedule/6/paragraph/9 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/schedule-6/paragraph-9
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.