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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).
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Information for developing and testing of software for HMRC forms, returns and messages.
Find out what goods you do not value when when working out the VAT due on import to the UK.
Get help classifying computers, inkjet and toner cartridges and their components.
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