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Guidance to help you manage the security of your devices and help protect your privacy
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
The Council for Science and Technology (CST) reports to the Prime Minister on science, engineering, technology and mathematics.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
How to distinguish between products that are regulated as medical devices and those regulated as medicinal products.
There are a number of high cost devices that are excluded from the Payment by Results (PbR) tariff.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
What you need to know about and do to comply with the law and keep consumers safe.
Information on when software applications are considered to be a medical device and how they are regulated.
Guidance for manufacturers, their authorised representatives and importers.
Choosing technology, development, integration, hosting, testing, security and maintenance.
Follow this guidance when you want to get spend approval for digital and technology activities.
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