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Biosimilars Council calls for more efficient regulatory pathways for critical medicines

A new position paper shows streamlining the approval process will foster advantages for patients, drug manufacturers and the FDA.

Budget Impact Analysis of Biosimilar Natalizumab in the US

Budget Impact Analysis of Biosimilar Natalizumab in the US
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PBM rebate schemes to suppress biosimilar Humira cost patients $6B, IQVIA analysis finds

The Biosimilars Council released a new analysis by IQVIA that reveals a PBM strategy to protect $2 billion in profits by “strangling” the biosimilar market and preventing savings for patients.

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