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Register to vote Register by 18 June to vote in the General Election on 4 July.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
This initiative signals an important step towards a new regulatory framework for medical devices in Great Britain which protects public health, ensures access to MedTech innovations, and maintains an attractive market for industry
Using smart meters to automate charging of electric vehicles.
Detention services order 05/2014 about the installation and removal of electronic monitoring devices from detainees.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
This guide is to help you and your business understand issues around data protection and privacy. It is intended for organisations that provide online services likely to be accessed by children.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
Posters and leaflets about using medical devices safely for healthcare professionals.
Guidance to assist fishers understand how and when I-VMS will be delivered in English waters, how it may affect them, their responsibilities, and the steps they need to consider.
Submissions related to human medicines need to be submitted directly to the MHRA.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
How to use a quasi-experimental study to evaluate your digital health product.
How the supply of medical devices from Great Britain into Northern Ireland works.
Guidance for device owners and installers on how to register energy devices, including heat pumps and electric vehicle charge points.
The home page for DSIT’s work supporting the secure and sustainable deployment of connected places technology, also known as smart cities.
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