# The Medicines (Products for Human Use) (Fees) Regulations 2016, Paragraph 5: Marketing authorisations


Unless paragraphs 6 to 10 apply, the fee payable under regulation 38(1) in connection with the holding of a marketing authorisation relating to a medicinal product of a kind described in column 1 of the following table is the applicable fee specified in the corresponding entry in column 2 of that table.
Periodic fees for holding a marketing authorisation
Column 1Type of Medicinal Product
Column 2Fee payable
1. New Active Substance
£11,627
2. Parallel Import
£368
3. Others
(a)
Any product (not being a derivative of a new active substance) in respect of which a marketing authorisation has been granted in consequence of a complex application submitted on or after 1st April 1989
£11,627
(b)
Prescription Only Medicine
(i)
Standard Fee
£2,908
(ii)
Reduced Rate Fee
£1,450
(iii)
Lower Fee
£368
(c)
Pharmacy
£368
(d)
General Sale List
£368
(e)
Herbal remedy
£92
(f)
Traditional herbal registrations
£92
(g)
National homoeopathic product
£92
(h)
Homoeopathic or anthroposophic product which is the subject of a licence of right
£92

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Source: https://www.legislation.gov.uk/uksi/2016/190/schedule/4/paragraph/5 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2016/schedule-4/paragraph-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.