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Register to vote Register by 18 June to vote in the General Election on 4 July.
Why to deploy regularly, deployment principles to follow, and how to do it.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Check a list of software developers who can provide Customs Declaration Service and Customs Handling of Import and Export Freight (CHIEF) software.
How to use usability testing to evaluate your digital health product.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
Understand your users and their needs. Develop knowledge of your users and what that means for your technology project or programme.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Supporting your team to make accessible services. Using semantic HTML, CSS, JavaScript and WAI-ARIA to make accessible interfaces.
Follow this guidance if you’re a civil servant or government contractor to use cloud tools safely.
If you manage an online platform that allows user generated content, these 7 steps will help you keep your business and your users safe.
This guidance outlines how to make informed choices about your organisation’s reliance on cloud technologies.
Find HMRC-recognised payroll software to manage your Real Time Information (RTI) PAYE payments and deductions.
How to use feedback from marketplace reviews to evaluate your digital health product.
Improve cross-departmental working by opening up access to video conferencing tools.
The Technology Code of Practice is a set of criteria to help government design, build and buy technology.
Manage, check and withdraw permission you've given to software applications to share and update your tax information
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Use open standards to build technology that is easier to expand and upgrade, and make sure it communicates with other technology.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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