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Medicines and Healthcare products Regulatory Agency - Activity on GOV.UK

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The Early Access to Medicines Scheme (EAMS) aims to give patients with life threatening or seriously debilitating conditions early access to medicines that show early signs of having a major advantage over existing therapeutics.

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Department of Health and Social Care and MHRA register of electronic export certificates (human).

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A list of individual human medicinal products under the new arrangements coming into effect on 1 January 2025 following agreement of the Windsor Framework.

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How to register on the MHRA portal and use it to apply for and update marketing authorisations and make other applications.

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As with all clinical trials, the MHRA’s top priority is the safety and wellbeing of the trial participants.

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