European Medicines Agency guidelines post December 31st.
What needs to change.

Pharmiweb - Cecilia Avram, Senior Regulatory Affairs Manager.

After months of Covid-related distractions, Brexit is back in the headlines - demanding new attention to how the life sciences industry will maintain cross-border product movement and manage regulatory administration from January 1.

Updated guidelines for pharmaceuticals marketing authorisation holders (MAHs) were published by EMA in March which will bring additional complexity, administration, cost and delay along the supply chain.

Cecilia Avram discusses the implications...

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