F1SCHEDULE 3PERIODIC FEES FOR LICENCES
F1PART 1Interpretation
F11
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F1PART 2Calculation of Turnover
Calculation of turnoverF12
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Manufacturer's pricesF13
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Evidence of turnoverF14
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F1PART 3Periodic Fees for Marketing Authorizations and Licences
Marketing authorizationsF15
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Marketing authorization: where Part 2 of the Act appliesF16
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Marketing authorization: derivativesF17
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Number of fee periodsF18
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Authorisation for two or more kinds of medicinal productF19
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Reduced feesF110
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Manufacturer's licences or manufacturing authorisationsF111
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Wholesale dealer's licencesF112
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Wholesale dealer's licences: evidenceF113
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Wholesale dealer's licences: exempt imported productsF114
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Additional amount for manufacturer's licences and wholesale dealer's licences which relate to exempt imported productsF115
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Clinical trial authorisationsF116
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Traditional herbal registrationsF117
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F1PART 4Types of Marketing Authorization for which only One Periodic Fee is Payable
Specified parallel import licencesF118
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Regulations revoked (1.4.2012) by The Medicines (Products for Human Use) (Fees) Regulations 2012 (S.I. 2012/504), regs. 1, 57(1) (with reg. 57(2)-(4)) and Regulations expressed to be revoked (N.I.) (1.4.2012) by The Medicines (Products for Human Use) (Fees) Regulations 2012 (S.R. 2012/134), regs. 1, 57 (with reg. 57(2)-(4))