# The Medicines (Products for Human Use) (Fees) Regulations 2010 (revoked)

S.I. 2010/551 · made 26 February 2010 · revised to 1 April 2012

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PDFs: Printed copy https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2010-revoked/pdf/uksi_20100551_en.pdf; Explanatory Memorandum https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2010-revoked/pdf/uksiem_20100551_en.pdf

## Introductory text

Medicines
Fees And Charges
Consumer Protection
Made 26th February 2010
Laid before Parliament 4th March 2010
Coming into force 1stApril 2010
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## Part 1: General

## 1 Citation and commencement

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## 2 Interpretation

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## Part 2: Capital Fees for Pre-Application Meetings

## 3 Interpretation of Part 2

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## 4 Fee for scientific advice: application for, or variation to, EU marketing authorization

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## 5 Fee for scientific advice: classification of a medicinal product

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## 6 Fee for advertising advice

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## 7 Fee for pharmacovigilance advice

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## 8 Fee for advice on labelling or leaflets

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## 9 Fee for regulatory advice

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## 10 Fee for advice for other purposes

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## 11 Time for payment of fees under regulations 4 to 10

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## Part 3: Capital Fees for Applications for Authorizations, Registrations, Licences, Certificates or Authorisations and for Associated Inspections

## 12 Fees for applications for authorizations, licences or certificates etc.

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## 13 Fee for applications for copy certificates of good manufacturing practice

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## 14 Fees for applications for certificates and copy certificates by exporters of medicinal products

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## Part 4: Capital Fees for Assistance in Obtaining Marketing Authorizations in Other EEA States

## 15 Meaning of “set of applications”

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## 16 Fees for applications for regulatory assistance under the mutual recognition procedure

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## 17 Time for payment of fees under regulation 16

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## Part 5: Capital Fees for Applications for Variations of Authorizations, Registrations, Licences and Authorisations and for Associated Inspections

## 18 Fees for variations of authorizations, registrations, licences and authorisations

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## 19 Fees for amendments to clinical trial authorisations

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## 20 Applications for multiple variations

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## Part 6: Capital Fees for Assessment of Labels and Leaflets

## 21 Meaning of “set of proposed changes”

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## 22 Fees for assessment of a set of proposed changes to labels and leaflets

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## 23 Time for payment of fees under regulation 22

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## Part 7: Capital Fees for Applications for Renewals of Certain Licences, Authorizations and Registrations and for Associated Inspections

## 24 Fees for renewals of certain manufacturer's licences

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## 25 Fees for renewals in terms which are not identical to the existing authorization, licence or registration

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## Part 8: Capital Fees for Regulatory Assistance Given by the United Kingdom Acting as Reference Member State Relating to the Assessment of Applications for the Renewal of Specified Marketing Authorizations

## 26 Fees for regulatory assistance for certain marketing authorizations

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## Part 9: Capital Fees for Inspections

## 27 Fees for inspections

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## 28 Payer of inspection fee (contract laboratories and API manufacturing sites)

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## 29 Inspections in connection with multiple applications

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## 30 Fees for inspections relating to good clinical practice in clinical trials

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## 31 Amount, and time for payment, of inspection fees in respect of an application for a wholesale dealer's licence

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## 32 Adjustment and refund of inspection fees in respect of a wholesale dealer's licence

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## Part 10: Periodic Fees for Authorizations, Registrations, Licences and Authorisations

## 33 Periodic fees

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## 34 Periodic fees for clinical trial authorisations

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## Part 11: Capital Fees For Application For Membership of Good Clinical Practice Accreditation Scheme and for Certificate of Membership

## 35 Meaning of “good clinical practice accreditation scheme”

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## 36 Fees for applications for membership and certificates

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## Part 12: Capital Fee for a Person Appointed Hearing

## 37 Fee for a person appointed hearing

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## 38 Time for payment under regulation 37

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## Part 13: Administration

## 39 Payment of fees to Ministers

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## 40 Time for payment of capital fees in connection with applications or inspections

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## 41 Time for payment of capital fees – applications made by small companies

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## 42 Payment of fees in respect of a traditional herbal registration

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## 43 Time for payment of periodic fees

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## 44 Penalty fees for late payment of periodic fees

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## 45 Daily penalty fees for late payment of periodic fees

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## 46 Refund or waiver of fees under regulation 44 or 45

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## 47 Adjustment, waiver, reduction or refund of fees

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## 48 Suspension of licences and authorisations

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## 49 Civil proceedings to recover unpaid fees

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## 50 Amendment of the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994

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## Part 15: Consequential Amendments

## 51 Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004

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## Part 16: Revocations and Savings

## 52 Revocations and savings

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## Signature

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## Schedule 1: CAPITAL FEES FOR APPLICATIONS FOR, AND VARIATIONS TO, MARKETING AUTHORIZATIONS, LICENCES, AUTHORISATIONS, REGISTRATIONS AND CERTIFICATES

### Part 1: General: interpretation and categories of applications and variations

## 1 Interpretation

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## 2 General: categories of Applications and Variations

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## 3 Administrative variation application

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## 4 Extension application

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## 5 Complex application

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## 6 Complex registration application

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## 7 Complex variation application

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## 8 Decentralised procedure application

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## 9 Extended Type II Complex Variation Application

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## 10 Major application

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## 11 Mutual recognition procedure incoming application

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## 12 New excipient variation application

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## 13 New indication variation application

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## 14 Parallel Import Licence application

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## 15 Reclassification variation application

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## 16 Reduced registration application

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## 17 Simple application

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## 18 Standard application

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## 19 Standard registration application

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## 20 Standard variation application

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## 21 Standard variation application for a homoeopathic medicinal product

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## 22 Type IB and Type II Applications

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## 23 Type II Complex Variation Application

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### Part 2: Capital Fees for Applications for Authorizations, Licences, Registrations and Certificates

## 24 Marketing authorizations

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## 25 Fees where application includes reclassification

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## 26 Fees where person holds clinical trial certificate

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## 27 Joint development

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## 28 Application for multiple authorizations

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## 29 Authorisation for a national homoeopathic product

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## 30 Manufacturer's licences and authorisations

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## 31 Wholesale dealer's licences

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## 32 Clinical trial authorisations

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## 33 Traditional herbal registrations

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### Part 3: Capital Fees for Assistance in Obtaining Marketing Authorizations in Other EEA States

## 34 Outgoing mutual recognition applications

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### Part 4: Capital Fees for Applications for Variations of Authorizations, Licences and Registrations

## 35 Marketing authorizations

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## 36 Variation of marketing authorizations

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## 37 Reclassification of marketing authorizations

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## 38 Variation of marketing authorization: national homoeopathic products

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## 39 Variation of parallel import licence

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## 40 Manufacturer's authorisations and licences

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## 41 Variation of manufacturer's authorisations and licences

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## 42 Wholesale dealer's licences

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## 43 Variation of wholesale dealer's licence

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## 44 Clinical trial authorisations

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## 45 Traditional herbal registrations

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## 46 Identical variations

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## 47 Complex Variation Applications

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## 48 Multiple reclassification variation applications

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### Part 5: Capital Fees for Assessment of Labels and Leaflets

## 49 A set of changes

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## 50 More than one set of charges proposed

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### Part 6: Capital Fees for Regulatory Assistance Given by the United Kingdom Acting as Reference Member State Relating to the Assessment of Applications for the Renewal of Specified Marketing Authorizations

## 51 Regulatory assistance

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## 52 Regulatory assistance – same manufacturer

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## Schedule 2: FEES FOR INSPECTIONS

## 1 General provisions relating to fees for inspections

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## 2 Fees: general

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## 3 Traditional herbal medicinal products

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## 4 Sites concerned with starting materials for traditional herbal medicinal products

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## 5 Wholesale dealer's licence: general

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## 6 Wholesale dealer's licence: traditional herbal medicinal products

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## 7 Wholesale dealer's licences: inspection of short duration

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## 8 Office-based inspections

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## Schedule 3: PERIODIC FEES FOR LICENCES

### Part 1: Interpretation

## 1 

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### Part 2: Calculation of Turnover

## 2 Calculation of turnover

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## 3 Manufacturer's prices

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## 4 Evidence of turnover

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### Part 3: Periodic Fees for Marketing Authorizations and Licences

## 5 Marketing authorizations

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## 6 Marketing authorization: where Part 2 of the Act applies

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## 7 Marketing authorization: derivatives

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## 8 Number of fee periods

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## 9 Authorisation for two or more kinds of medicinal product

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## 10 Reduced fees

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## 11 Manufacturer's licences or manufacturing authorisations

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## 12 Wholesale dealer's licences

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## 13 Wholesale dealer's licences: evidence

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## 14 Wholesale dealer's licences: exempt imported products

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## 15 Additional amount for manufacturer's licences and wholesale dealer's licences which relate to exempt imported products

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## 16 Clinical trial authorisations

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## 17 Traditional herbal registrations

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### Part 4: Types of Marketing Authorization for which only One Periodic Fee is Payable

## 18 Specified parallel import licences

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## Schedule 4: TIME FOR PAYMENT OF CAPITAL FEES

## 1 Interpretation

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## 2 Major application

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## 3 Complex application

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## 4 Multiple application

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## 5 Outgoing mutual recognition application

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## 6 Application for traditional herbal registration

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## 7 Traditional herbal registration: complex variation

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## 8 Application for manufacturer's licence, manufacturing authorisation or wholesale dealer's licence

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## 9 Inspection fees in connection with applications

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## Schedule 5: WAIVER, REDUCTION OR REFUND OF CAPITAL FEES

## 1 Interruptions of manufacture, assembly, sale or supply

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## 2 Reclassification

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## 3 Variation of a traditional herbal registration

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## 4 Withdrawal of application in relation to marketing authorization, traditional herbal registration or clinical trial authorisation

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## 5 Withdrawal of application in relation to manufacturing authorisation, wholesale dealer's licence or manufacturer's licence

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## 6 Refusal of application for grant of marketing authorization, traditional herbal registration or clinical trial authorisation

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## 7 Parallel import licence

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## 8 Surrender of marketing authorization at same time as a variation application

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## 9 Clinical trial authorisation

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## 10 Scientific advice: paediatric indications

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## Schedule 6: ADJUSTMENT, REDUCTION OR REFUND OF PERIODIC FEES

## 1 Refund on surrender or revocation of authorization, registration or licence

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## 2 Adjustment and refund: licences relating to exempt imported products

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## 3 Refunds: treated as having been paid on account

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## Schedule 7: INTERPRETATION

## 1 Interpretation

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## 2 

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## 3 

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## Explanatory note

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Source: https://www.legislation.gov.uk/uksi/2010/551 (the official version)
Page: https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2010-revoked
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

