UK Statutory Instrument
2025
United Kingdom
The Human Medicines (Authorisation by Pharmacists and Supervision by Pharmacy Technicians) Order 2025
At a glance
Enforced by
What this Act requires
Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.
Browse 12 other sections — procedural / definitional / commencement
Extent
Privy Council procedures and legislative procedures
Exemption from requirement for manufacturer’s licence or marketing authorisation: authorisation of a pharmacist
Exemption from the requirement for manufacturer’s licence or marketing authorisation: registered pharmacy technicians at hospital aseptic facilities
Assembly of investigational medicinal products in hospitals and health centres
Exemptions from prohibition on sale or supply of medicinal products not subject to general sale: two types of authorisation of a pharmacist
Standards of conduct, ethics and performance related to authorisations
Consequential amendments to the Misuse of Drugs (Safe Custody) Regulations 1973
Consequential amendments to the Misuse of Drugs Regulations 2001
Consequential amendment to the Medicines for Human Use (Clinical Trials) Regulations 2004
Consequential amendments to the Human Medicines Regulations 2012 and transitional provision
Enforcement and responsible bodies
The regulators that administer or enforce this legislation.
General Pharmaceutical Council
Statutory regulator for pharmacists, pharmacy technicians, and pharmacy premises in Great Britain. Sets standards for pharmacy education, ethics, and practice. Inspects registered …
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Regulators
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