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In the spring of 2022, the Food and Drug Administration (FDA) approved tirzepatide for the management and treatment of T2DM, and it has also recently been approved in Europe

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As the demand for GLP-1s is expected to stir competition in the global pharma CDMO market, CDMOs may look to prioritise lucrative contracts and non-GLP-1 drugs may experience disruption as they struggle to source fill-finish services, primary packaging, and single-use technologies

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They will play a decisive role in market access and will be a key negotiating interface between manufacturer and distributor