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

http://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/29/made

The Human Medicines Regulations 2012

Medicines

Management information systems

Motor industry

King's Printer of Acts of Parliament

2016-09-14

MEDICINES

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

29

The licence holder must not use any premises for the handling, storage or distribution of medicinal products other than those specified in the licence or notified to the licensing authority from time to time and approved by the licensing authority.