# The Medicines (Fees Relating to Medicinal Products for Human Use) Amendment Regulations 1990, Regulation 4: Amendment of regulation 3 of, and additional regulation 3A to, the principal Regulations


(1) In regulation 3 of the principal Regulations (applications for licences) for the words “Subject to regulations 16 and 20”, there shall be substituted “Subject to regulations 3A, 16 and 20”.
(2) After regulation 3 there shall be inserted the following regulation—
“Inspections in connection with multiple applications for licences
3A Where an inspection mentioned at regulation 3(b) of these Regulations is made at a site which has been named as a possible site for manufacture of a medicinal product by more than one applicant for—
(a) a product licence and that site is located outside the United Kingdom; or
(b) a manufacturer’s licence and that site is located in the United Kingdom,
the fee in respect of that inspection shall be payable in equal proportions by each applicant for such licence.”.

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Source: https://www.legislation.gov.uk/uksi/1990/210/regulation/4 (the official version)
Page: https://openlegislation.uk/medicines-fees-relating-to-medicinal-products-for-human-use-amendment-regulations-1990/regulation-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.