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Dec 27, 20232 min read

UK MHRA: Guidance on Submitting Changes to Labelling and Patient Information Leaflets

On 22nd December 2023, the Medicines and Healthcare Products Regulatory Agency (MHRA) updated its guidance on Medicines "Submitting...

Jun 13, 20211 min read

Open Consultation for EU common standard on electronic product information- EMA

The European Medicines Agency (EMA) on 8th June 2021 launched a stakeholder consultation on a draft EU common standard for electronic...