# The Medicines (Products for Human Use) (Fees) Regulations 2012, Regulation 8: Fee for advice on labelling or leaflets


The fee payable by the holder of one or more marketing authorizations with whom the licensing authority holds a meeting in order to provide advice on proposed changes to the labelling or the package leaflets of the medicinal products to which those authorizations relate, is £2,378.

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Source: https://www.legislation.gov.uk/nisr/2012/134/regulation/8 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/regulation-8
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.