# The Medicines (Products for Human Use) (Fees) Regulations 2012, Paragraph 41: Variation of manufacturer’s authorisations and licences


The fee payable under regulation 18(1)(c) or (d) in connection with an application for variation of a manufacturing authorisation or a manufacturer’s licence is £250 in respect of each variation applied for which constitutes a change to the authorisation or licence not requiring an inspection or medical, scientific or pharmaceutical assessment.

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Source: https://www.legislation.gov.uk/nisr/2012/134/schedule/2/paragraph/41 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/schedule-2/paragraph-41
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.