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

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How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.

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List of Field Safety Notices from 7 September to 11 September 2026.

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How to get a marketing authorisation (MA) for an advanced therapy medicinal product (ATMP) so it can be sold and/or supplied in the United Kingdom.

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New recommendations based on extensive public engagement set out how the NHS could give patients faster access to AI advances with proportionate safeguards to protect patient safety and maintain high levels of trust.

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Recommendations from the National Commission into the Regulation of AI in Healthcare, which was established to advise government on a future regulatory framework for AI in healthcare.

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