The Medicines (Products for Human Use) (Fees) Regulations 2016
These Regulations revoke and re-enact, with some amendments, the Medicines (Products for Human Use) (Fees) Regulations 2013 (“the 2013 Regulations”). They make amendments to the Medical Devices (Consultation Requirements) (Fees) Regulations 1995 (“the 1995 Regulations”).
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Lifecycle
Department
Made
11 Feb 2016
—
In force
01 Apr 2016
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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