http://www.legislation.gov.uk/id/uksi/2019/775

http://www.legislation.gov.uk/uksi/2019/775/regulation/141

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

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EXITING THE EUROPEAN UNION

MEDICINES

Statute Law Database

2024-05-16

Expert Participation

2021-08-03

These Regulations are made in exercise of the powers conferred by section 8(1) of the European Union (Withdrawal) Act 2018 (c. 16) in order to address failures of retained EU law to operate effectively and other deficiencies (in particular under section 8(2)(a), (b), (c), (d), (f) and (g) and (6)) arising from the withdrawal of the United Kingdom from the European Union. They are also made under paragraphs 1(1) and 7(2) of Schedule 4 to the European Union (Withdrawal) Act 2018, insofar as they make provision in relation to fees.

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

reg. 17(4)

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

Sch. 1

para. 3

reg. 1

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

PART 11Amendment of Part 11 (Pharmacovigilance)

F1Amendment of regulation 181 (delegation of obligations under Part 11)I1141

In regulation 181(1), for “to another EEA State” substitute “in connection with its pharmacovigilance system in relation to medicinal products for sale or supply in Northern Ireland to an EEA State”.

Annotations:

Commencement Information

Reg. 141 in force at 31.12.2020 on IP completion day (in accordance with 2020 c. 1, Sch. 5 para. 1(1)), see reg. 1

Amendments (Textual)

Reg. 141 substituted (31.12.2020 immediately before IP completion day) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1488), reg. 1, Sch. 2 para. 110