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Register to vote Register by 18 June to vote in the General Election on 4 July.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
A lesson in exceeding the original concept: The journey of Createc's LiDAR autonomous crowd monitoring solution, purchased by Network Rail
Advice on writing clear notices and maximising replies to your FSNs.
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
VRAI secured a DASA Defence Innovation Loan to help commercialise their data capture and analysis technology to help the RAF rapidly assess airmanship in future aviators
How GBN’s technology selection process for Small Modular Reactors (SMRs) will work.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
A beginner's guide on assessing whether a proposed housing project is financially viable.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Thousands of counterfeit or unbranded copies of LifeVac anti-choking devices are being sold across the UK. The public is reminded to check their product carefully against the images in MHRA guidance to identify whether it is a counterfeit.
Information on the National Underground Asset Register (NUAR).
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
Guidance for businesses.
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
This is collated guidance from government websites and independent bodies to help you follow the technology code of practice.
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