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This consultation seeks views on amending the Human Medicines Regulations 2012 to support the ongoing supply and deployment of vaccinations across the UK.
This is the original consultation document. Executive summary In response…
Introduction In response to the COVID-19 pandemic, multiple regulations…
Proposal to make a permanent order to prevent new patients aged under 18 from beginning to take puberty blockers for the purposes of gender incongruence and/or gender dysphoria, under the care of private prescribers.
Introduction Gender incongruence and/or gender dysphoria are conditions…
Introduction The general equality duty that is set out in the Equality Act…
Background On 20 August 2024, a targeted consultation was issued on…
We are seeking feedback on our new draft guideline on individualised mRNA cancer immunotherapies, a new type of cancer treatment being tested in clinical trials. This will help us to clarify and streamline pathways for bring…
This consultation seeks views on extending medicines responsibilities for paramedics, physiotherapists, operating department practitioners and diagnostic radiographers.
We invite feedback on the operation and impact of the human medicines and medical devices legislation as part of a statutory review required under the Medicines and Medical Devices Act 2021.
MHRA seeks views on possible amendments to the Medical Devices Regulations 2002 to include common specification requirements for manufacturers of IVD devices.
Factsheet providing more information on the Commission on Human Medicines' independent report on the safety implications of proposed puberty blocker legislation.
Policy statement setting out case studies for the sale of hearing aids in the UK.
Government’s response to the independent review into racial, ethnic and other factors leading to unfair biases in the design and use of medical devices.
First published during the 2022 to 2024 Sunak Conservative government
We are seeking your views on the design, development, evaluation and use of medical devices.
First published during the 2019 to 2022 Johnson Conservative government
Report on all regulations in force during the first reporting period made using the powers in specific sections of the act, including stakeholder feedback and the department’s response.
Seeks views on proposed changes to regulations 3A, 19 and 247A of the Human Medicines Regulations 2012 to support the ongoing delivery of COVID-19 and influenza vaccination.
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
A report summarising the findings following a one-year review of the use of regulations 174A and 247A, implemented to support the rollout of COVID-19 and flu vaccines.
We would like your views on a review of temporary provisions in the Human Medicines Regulations to support influenza and COVID-19 vaccination campaigns.
Impact assessment evaluating the measures in the Medicines and Medical Devices Bill, and illustrative statutory instruments showing how powers in the bill may be used.
We are asking for views on a new draft version on our guidance for users, carers and staff on the safe use of bed rails.
This consultation invites views on the proposed steps we intend to take to make sure the UK meets its obligations to transpose the 'safety features' provisions of the Falsified Medicines Directive (FMD).
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