We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Register to vote Register by 18 June to vote in the General Election on 4 July.
Information on when software applications are considered to be a medical device and how they are regulated.
Advice for manufacturers, members of the public and professional users of software or apps being used during the COVID-19 pandemic.
The team capabilities available on the Digital Outcomes framework.
Information for developing and testing of software for HMRC forms, returns and messages.
How to manage configuration: open source tools, writing infrastructure in code, portability.
Descriptions of team capabilities on the Digital Outcomes and Specialists framework.
How to send information to Companies House through our extensible markup language (XML) schemas, by purchasing software or developing your own.
Find a list of simple record keeping applications, including cash basis and simplified expenses specifications.
The Crown Commercial Service technology service principles help us to continually improve the way technology is bought across government and the public sector.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
The Medicines and Healthcare products Regulatory Agency (MHRA) have embarked upon an ambitious programme of reform to ensure that medical device regulation is fit for purpose for software, including artificial intelligence (AI).
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).