Mhra 2025 Schedule. From 1 january 2025, all medicines approved in the uk will be licensed by the mhra and authorised under the human medicines regulation 2012 (as amended) (hmrs). With industry already showing a very high level of readiness,.


Mhra 2025 Schedule

The uk medicines and healthcare products regulatory agency (mhra) has published new guidance for pharmaceutical manufacturers and wholesalers in order to implement the arrangements of the windsor. Click here for the new deadlines, requirements & link to the roadmap.

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