The UK government has issued guidance explaining the new labeling requirements for medicines that are licensed on a UK-wide basis as of 1 January 2025, noting that companies wanting to comply with the rules before that date are welcome to do so.
The key requirements for medicines under the so-called “Windsor Framework” agreed by the UK and the EU in February is that all new products that currently fall within the scope of the EU centralized procedure will need to be authorized for the whole of the UK (England, Northern
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