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Threads / Human Medicines Regulations Amendments / Timeline

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Human Medicines Regulations Amendments

The Department of Health and Social Care and MHRA are amending the Human Medicines Regulations through draft regulations and consultation on changes to health service product information disclosure rules, aimed at benefiting NHS patients and British businesses through modernised medicines access procedures. The amendments represent significant changes to the regulatory framework governing medicines approval and provision.

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Key signals 96 All signals 133 Consultations 88 Policy and strategy 6 Legislative record 3 Scrutiny and evidence 16 Analysis 1 Announcements 19

Family 1

Consultations 88 Policy and strategy 6 Legislative record 3 Scrutiny and evidence 16 Analysis 1 Announcements 19

Signal

Open Consultations 10 Closed Consultations 9 Consultation Responses 67 Government responses 2 Policy papers 6 Bill / Act text 1 Bill stages 2 Statements and announcements 19 Impact assessments 1 Written questions 16

Year

2026 22 2025 11 2024 18 2023 17 2022 16 2021 11 2020 5 2019 1 2018 7 2017 4 2016 3 2015 9 2014 6 2013 3

Body

Commission on Human Medicines 4 Department of Health and Social Care 110 Foreign, Commonwealth & Development Office 1 Medicines and Healthcare products Regulatory Agency 36

Role

Analysis / research (departmental, academic, briefings) 1 Consultation (this thread's consultation) 88 Instrument (the named Bill / Act / SI / Code) 1 Parliamentary record (Hansard debates, PQs, statements) 37 Strategy / programme document (e.g. CAM 2025) 6

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Family: Analysis ×

25 Jan 2022 | Impact assessment Department of Health and Social Care linked

Review of temporary provisions in the Human Medicines Regulations 2012 to support COVID-19 and influenza vaccination campaigns: equality impact assessment

In response to: Review of temporary provisions in the Human Medicines Regulations 2012 to support influen…

▤ View document · ↗ GOV.UK

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Ownership

Government Department

Dept Department of Health and Social Care

Dept Medicines and Healthcare products Regulatory Agency

About this issue

Last updated

6 May 2026

Events

1

Departments

2

Status

Closed

Themes

Healthcare & life sciences

Policy Threads

UK policy issues — from consultation to statute, in one thread.

About & methodology

Documents sourced from GOV.UK, Parliament, devolved governments and statutory regulators under the Open Government Licence v3.0 or equivalent.

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