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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
New satellite-enabled ankle tags are being rolled out in phases across England and Wales by the Ministry of Justice.
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
It’s illegal to hold a phone or a sat nav while driving - you'll get penalty points, a fine and can be banned from driving.
Information about the EU Regulations and their implementation in Northern Ireland
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to conform with the legal requirements for placing medical devices on the market.
I-VMS - Frequently asked questions
This inspection examined the Global Positioning System (GPS) electronic monitoring of Foreign National Offenders, with a particular focus on the processing and flow of information through the Electronic Monitoring Hub from September 2021 to March 2022.
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.
The Government Procurement Service (GPS) is now part of the Crown Commercial Service, a new organisation which also includes the former commercial function of the Cabinet Office, and common goods and services procurement and commercial management currently undertaken by departments.
Using an ecological momentary assessment to evaluate your digital health product.
Order a certificate of free sale to export medical devices outside the UK.
Manufacturers should use these forms when a device is released to a vessel owner and to confirm a device has been installed and is working.
Using recommended patterns for workplace wifi networks and sharing infrastructure.
This process evaluation report explores views and experiences of the implementation and delivery of the GPS Electronic Monitoring pilot.
Explains what local authorities should do before publishing their data.
The MHRA has conducted a thorough assessment of technical and biological safety information provided by NSO and is satisfied that the modified MAGEC X system can now be used in the UK.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
How to support patients in accessing population screening programmes and obtaining screening results.
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