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The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024

Table of Contents
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Draft Explanatory Memorandum
Draft Explanatory Memorandum
Draft Explanatory Memorandum sets out a brief statement of the purpose of a Draft Statutory Instrument and provides information about its policy objective and policy implications. They aim to make the Draft 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.
Draft Impact Assessments
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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Draft Legislation:

This is a draft item of legislation. This draft has since been made as a UK Statutory Instrument: The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024 No. 1368

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