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Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
Information and guidance on a range of medical devices for users and patients.
The government’s plan to build a circular economy for medical technology to increase resilience, drive growth, realise cost savings and improve sustainability.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
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