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How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Resources to help local commissioners achieve value for money by estimating the return on investment (ROI) and cost-effectiveness of public health programmes.
How branding and bidding occurs, how this process has become vital in securing foreign aid to run MCH activities in Nepal
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
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