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There are currently no known outstanding effects for the The Medicines (Products for Human Use) (Fees) Regulations 2012 (revoked).
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PART 4 Capital Fees for Assistance in Obtaining Marketing Authorizations in Other EEA States
PART 9 Capital Fees for Inspections
28.Payer of inspection fee (contract laboratories and API manufacturing sites)
30.Fees for inspections relating to good clinical practice in clinical trials
31.Amount, and time for payment, of inspection fees in respect of an application for a wholesale dealer's licence
32.Adjustment and refund of inspection fees in respect of a wholesale dealer's licence
PART 10 Periodic Fees for Authorizations, Registrations, Licences and Authorisations
PART 1 General: interpretation and categories of applications and variations
PART 2 Capital Fees for Applications for Authorizations, Licences, Registrations and Certificates
PART 3 Capital Fees for Assistance in Obtaining Marketing Authorizations in Other EEA States
PART 4 Capital Fees for Applications for Variations of Authorizations, Licences and Registrations
WAIVER, REDUCTION OR REFUND OF CAPITAL FEES
4.Withdrawal of application in relation to marketing authorization, traditional herbal registration or clinical trial authorisation
5.Withdrawal of application in relation to a certificate of registration
6.Withdrawal of application in relation to manufacturing authorisation, wholesale dealer's licence or manufacturer's licence
7.Refusal of application for grant of marketing authorization, traditional herbal registration or clinical trial authorisation
9.Surrender of marketing authorization at same time as a variation application
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