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Information about COVID-19 and pregnancy from the Royal College of Obstretricians and Gynaecologists (RCOG).
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to use a feasibility study when planning the evaluation of your digital health product.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
How to use the GOV.UK ID Check app to prove your identity, including how to download the app and how to scan your face and your photo ID.
PC Ady Bebb successfully broke the Guinness World Record for ‘Fastest Marathon dressed as a Road Vehicle’ during the London Marathon recently.
Information and guidance on a range of medical devices for users and patients.
Check the tariff classification for all kinds of watch straps, watch bands and watch bracelets used for fastening watches to the wrist.
The CMA is investigating Google’s conduct in relation to Google’s distribution of apps on Android devices in the UK, in particular Google Play’s rules which oblige certain app developers to use Google Play’s own billing system for in-app purchases.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Find out about the long-term effects some people can have after having COVID-19.
How to use a case-control study to evaluate your digital health product.
Find out how the accessibility monitoring methodology is used to test websites and mobile apps under the Accessibility Regulations
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
This guidance is designed to help schools ensure they have the correct devices required to deliver the 2025 reception baseline assessment (RBA).
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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