Welcome to the About us section.
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The Medicines and Healthcare products Regulatory Agency (MHRA) is the government agency which is responsible for ensuring that medicines and medical devices work, and are acceptably safe.
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No product is risk-free. Underpinning all our work lie robust and fact-based judgements to ensure that the benefits to patients and the public justify the risks.
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We keep watch over medicines and devices, and we take any necessary action to protect the public promptly if there is a problem.
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We aim to make as much information as possible publicly available.
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We enable greater access to products, and the timely introduction of innovative treatments and technologies that benefit patients and the public.
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We encourage everyone - the public and healthcare professionals as well as industry - to tell us about any problems with a medicine or medical device, so that we can investigate and take any necessary action.
A full explanation of what we do and how we do it is in our publication:
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'Medicines & Medical Devices Regulation: What you need to know'