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A buyer's guide for mobile devices, which outlines 7 areas that consumers should check for when choosing or using their mobile device.
Guidance for manufacturers, importers and distributors (including retailers).
Guidance for manufacturers on placing batteries and accumulators on the market.
This document provides the security framework for government end user devices using official government information.
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
Information on when software applications are considered to be a medical device and how they are regulated.
Find out about the VAT domestic reverse charge procedure which applies to the buying and selling of certain goods and services.
Industry update on the results of I-VMS device testing, as MMO confirms its ongoing commitment to support fishers.
Advice and guidance on the management and use of point-of-care testing (POCT) in vitro diagnostic (IVD) devices.
Home Office approved breath alcohol analysis testing devices.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Guidance on the use of personal protective equipment (PPE) for aerosol generating procedures (AGPs).
The Interim Devices Working Group replaces the Devices Expert Advisory Committee (DEAC) and is responsible for providing independent, external expert input and advice on a wide range of aspects relating to medical devices to help MHRA ensure the safe introduction...
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