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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.
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.
Descriptions of team capabilities on the Digital Outcomes and Specialists framework.
The team capabilities available on the Digital Outcomes framework.
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.
How to send information to Companies House through our extensible markup language (XML) schemas, by purchasing software or developing your own.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
Check a list of software developers who can provide Customs Declaration Service and Customs Handling of Import and Export Freight (CHIEF) software.
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