http://www.legislation.gov.uk/id/uksi/2012/1916/schedule/24

http://www.legislation.gov.uk/uksi/2012/1916/schedule/24/paragraph/52

The Human Medicines Regulations 2012

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text/xml

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)

SCHEDULES

SCHEDULE 24Packaging information requirements

F1PART 5Immediate packaging: blister packs and small packaging (advanced therapy medicinal products for sale or supply in Great Britain only)

Annotations:

Amendments (Textual)

Sch. 24 Pts. 4, 5 inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), regs. 1, 201(5) (as amended by S.I. 2020/1488, reg. 1, Sch. 2 para. 155(d)); 2020 c. 1, Sch. 5 para. 1(1)

52

The unique donation code assigned by a tissue establishment pursuant to—

a

paragraph 1 of Schedule 3A to the Human Fertilisation and Embryology Act 1990, as regards human gametes and embryos; and

b

paragraph 1 of Schedule 2 to the Human Tissue (Quality and Safety for Human Application) Regulations 2007, as regards other human tissues and cells.