# The Medicines (Fees Relating to Medicinal Products for Human Use) Amendment (No. 2) Regulations 1990, Regulation 4: Amendment of Part I of Schedule 1 to the principal Regulations


In Schedule 1 to the principal Regulations (fees for applications, variations and renewals of licences), in paragraph 1 in Part I (interpretation), after the definition of “product licence (parallel import)”, there shall be inserted the following—
““qualified person” means the person named in the licence as being the person who is to carry out the functions specified in paragraph 16(3) of Schedule 2 to the Medicines (Standard Provisions for Licences and Certificates) Regulations 1971 in relation to a manufacturer’s licence or paragraph 8 of Schedule 3 to those Regulations in relation to a wholesale dealer’s licence;”.

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Source: https://www.legislation.gov.uk/uksi/1990/2326/regulation/4 (the official version)
Page: https://openlegislation.uk/medicines-fees-relating-to-medicinal-products-for-human-use-amendment-no-2-regulations-1990/regulation-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.