- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (a wnaed Fel)
There are currently no known outstanding effects for the The Medicines (Products for Human Use) (Fees) Regulations 2013 (revoked).
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
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
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.
Mae Memoranda Esboniadol yn nodi datganiad byr o ddiben Offeryn Statudol ac yn rhoi gwybodaeth am ei amcan polisi a goblygiadau polisi. Maent yn ceisio gwneud yr Offeryn Statudol yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol, ac maent yn cyd-fynd ag unrhyw Offeryn Statudol neu Offeryn Statudol Drafft a gyflwynwyd ger bron y Senedd o Fehefin 2004 ymlaen.
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