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Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Order a certificate of free sale to export medical devices outside the UK.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
How to get fast-track approval of medical devices during COVID-19.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Information about the EU Regulations and their implementation in Northern Ireland
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
You must not supply certain single-use plastic items in England, except for some exemptions.
Find out which supplies of children’s clothing or footwear are zero-rated for VAT.
How the supply of medical devices from Great Britain into Northern Ireland works.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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