Chapter 1 Regulations: generalF1
- 2Power to make regulations about human medicines
- 3Manufacture, marketing and supply
- 4Falsified medicines
- 5Clinical trials
- 6Fees, offences, powers of inspectors
- 7Emergencies
Annotations
Textual amendments
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Pt. 2 Ch. 1 heading substituted (1.7.2022) by Health and Care Act 2022 (c. 31), ss. 101(2), 186(6); S.I. 2022/734, reg. 2(a), Sch. (with regs. 13, 29, 30)