http://www.legislation.gov.uk/id/uksi/2012/1916

http://www.legislation.gov.uk/uksi/2012/1916/regulation/32

The Human Medicines Regulations 2012

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Statute Law Database

MEDICINES

2024-05-20

Expert Participation

2024-03-31

These Regulations consolidate the law of the United Kingdom concerning medicinal products for human use (“products”) in respect of the topics described below.

The Human Medicines Regulations 2012

reg. 51(9)

The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019

Sch. 1

para. 5

reg. 1

The Human Medicines Regulations 2012

reg. 52(1)(a)(i)(ii) and words

The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019

reg. 57(2)

reg. 1

The Human Medicines Regulations 2012

reg. 53(2)-(2C)

The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019

reg. 58(3)

reg. 1

The Human Medicines Regulations 2012

reg. 53(2)(a)

The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019

Sch. 1

para. 6(2)

reg. 1

The Human Medicines Regulations 2012

Sch. 11

para. 1(1)(d)-(f)

The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019

reg. 63(2)(a)(ii)

reg. 1

The Human Medicines Regulations 2012

Sch. 33A

para. 57(2)

The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019

Sch. 1

para. 10(3)(a)

reg. 1

The Human Medicines Regulations 2012

Sch. 33A

para. 57(3)

The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019

Sch. 1

para. 10(3)(b)

reg. 1

The Human Medicines Regulations 2012

Sch. 33A

para. 57A

The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019

Sch. 1

para. 10(4)

reg. 1

The Human Medicines Regulations 2012

reg. 173(e)

The Ionising Radiation (Medical Exposure) Regulations 2017

Sch. 4

para. 2(2)(b)

reg. 1

The Human Medicines Regulations 2012

reg. 240(2A)

The Ionising Radiation (Medical Exposure) Regulations 2017

Sch. 4

para. 2(3)(c)

reg. 1

The Human Medicines Regulations 2012

reg. 240(6A)

The Ionising Radiation (Medical Exposure) Regulations 2017

Sch. 4

para. 2(3)(g)

reg. 1

The Human Medicines Regulations 2012

reg. 217BA

The Human Medicines (Amendment Relating to Original Pack Dispensing) Regulations (Northern Ireland) 2024

reg. 2(2)

reg. 1(2)

The Human Medicines Regulations 2012

reg. 217CA

The Human Medicines (Amendment Relating to Original Pack Dispensing) Regulations (Northern Ireland) 2024

reg. 2(3)

reg. 1(2)

PART 3F1Manufacture and distribution of medicinal products and active substances

Annotations:

Amendments (Textual)

Pt. 3 heading and Pt. 3 Ch. 1 inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4

F2CHAPTER 2Manufacturing and wholesale dealing

Annotations:

Amendments (Textual)

Pt. 3 Ch. 2 heading inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4

Miscellaneous and offences

Sale and supply of starting materialsF332

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