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The MHRA regulates the approval of new medicines in Great Britain following the UK's departure from the European Union, whilst the EMA retains responsibility for authorisation across EU member states

Despite sustained innovation across multiple technological generationssuch as enteric coatings, enzyme inhibitors, permeation enhancers, nanoparticles, and ingestible devicesmost oral peptide programs have failed to achieve regulatory or commercial success

Consulting with healthcare providers ensures appropriate use and monitoring

But once youre pregnant, the official guidance is to stop taking the medication