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is importing so many weight-loss and diabetes drugs that its distorting trade data
In simple terms, it determines which raw ingredients (bulk drug substances) can be legally used to create compounded medications when a patient needs a customized formulation and there is no suitable FDA-approved product available
This personalized contextcombined with biomarker monitoring and close clinical supervisionstrengthens shared decision-making in a complex clinical situation
Ragab SM, Aboelnga MM, Moawed EA, El Sadda RR, Khairy GM
Europe: Earlier biosimilar competition possible due to different patent laws
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