The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2012 (revoked)
These Regulations amend the Medicines (Products for Human Use) (Fees) Regulations 2012 (“the 2012 Regulations”). The 2012 Regulations make provision for the fees payable under the Medicines Act 1971 and other fees payable in respect of EU obligations relating to marketing authorisations, licences and certificates in respect of medicinal products for human use.
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Lifecycle
Department
Made
04 Oct 2012
—
In force
02 Nov 2012
Enabling power
In accordance with section 129(6) of the Medicines Act 1968, the Secretary of State for Health and the Minister for Health, Social Services and Public Safety have consulted with such organisations as appear to them to be representative of interests likely to be substantially affected by these Regulations.
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