# The Medicines (Products for Human Use) (Fees) Regulations 2012, Regulation 13: Fee for applications for copy certificates of good manufacturing practice


The fee payable by an applicant for a certified copy of a certificate of good manufacturing practice issued pursuant to Article 111(5) of the 2001 Directive is £67.

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Source: https://www.legislation.gov.uk/nisr/2012/134/regulation/13 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/regulation-13
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.