- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/04/2013)
- Gwreiddiol (a wnaed Fel)
There are currently no known outstanding effects for the The Medicines (Products for Human Use) (Fees) Regulations 2013 (revoked).
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PART 4 Capital Fees for Assistance in Obtaining Marketing Authorisations in Other EEA States
PART 9 Capital Fees for Inspections
30.Fees for inspections of pharmacovigilance service providers
31.Payer of inspection fee (contract laboratories and API manufacturing sites)
33.Fees for inspections relating to good clinical practice in clinical trials
34.Amount, and time for payment, of inspection fees in respect of an application for a wholesale dealer's licence
35.Adjustment and refund of inspection fees in respect of a wholesale dealer's licence
36.Amount, and time for payment, of inspection fees in respect of an application for a broker's registration or an active substance registration
PART 10 Periodic Fees for Authorisations, Registrations and Licences
PART 12 Capital Fee for a Review Upon Oral Representations or a Person Appointed Hearing
SCHEDULES
PART 1 General: interpretation and categories of applications and variations
PART 2 Capital Fees for Applications for Authorisations, Licences, Registrations and Certificates
PART 3 Capital Fees for Assistance in Obtaining Marketing Authorisations in Other EEA States
PART 4 Capital Fees for Applications for Variations of Authorisations, Licences and Registrations
Waiver, reduction or refund of capital fees
4.Withdrawal of application in relation to marketing authorisation, 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, manufacturer's licence, broker's registration or active substance registration
7.Refusal of application for grant of marketing authorisation, traditional herbal registration or clinical trial authorisation
9.Surrender of marketing authorisation at same time as a variation application
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