The Human Medicines (Amendment) (No. 3) Regulations 2015

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The Human Medicines (Amendment) (No. 3) Regulations 2015

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Explanatory Memorandum

Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Instrument and provides information about its policy objective and policy implications. They aim to make the Statutory Instrument accessible to readers who are not legally qualified and accompany any Statutory Instrument or Draft Statutory Instrument laid before Parliament from June 2004 onwards.

Impact Assessments

Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:

Why the government is proposing to intervene;
The main options the government is considering, and which one is preferred;
How and to what extent new policies may impact on them; and,
The estimated costs and benefits of proposed measures.

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Introductory Text
1.Citation and commencement
2.Amendment of the Human Medicines Regulations 2012
3.Amendment of regulation 8
4.Amendment of regulation 38
5.Amendment of regulation 39
6.Amendment of regulation 44
7.Amendment of regulation 233
8.Amendment of regulation 256E
9.Amendment of regulation 346
10.Amendment of Schedule 17
Signature
Explanatory Note

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The Human Medicines (Amendment) (No. 3) Regulations 2015

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Explanatory Memorandum

Impact Assessments

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