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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The Medicines and Healthcare products Regulatory Agency (MHRA), working with law enforcement partners, seized more than 15.5 million doses of illegally traded medicines with a street value of more than £30 million during 2023.
Information about the EU Regulations and their implementation in Northern Ireland
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Information and guidance on a range of medical devices for users and patients.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to get an ENG1 or ML5 medical certificate.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Medical advisory panels work with DVLA to provide expert advice, with the aim of improving road safety. See information on their role and current vacancies.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for NHS regarding disclosure to individuals holding either a Lasting Power of Attorney or a deputyship.
How to conform with the legal requirements for placing medical devices on the market.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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