http://www.legislation.gov.uk/id/uksi/2012/1916/schedule/4

http://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/30

The Human Medicines Regulations 2012

text

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

SCHEDULES

SCHEDULE 4Standard provisions of licences under Part 3

PART 4Wholesale dealer's licence

All wholesale dealer's licences

30

The licence holder must provide such information as may be requested by the licensing authority concerning the type and quantity of medicinal products which the licence holder handles, stores or distributes.