Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
EMA Confirms Usefulness of Pioglitazone-Containing Medicines as 2nd, 3rd Line Treatment Options: Takeda
The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) clarified on October 21 the label changes for the type 2 diabetes treatment Actos (pioglitazone) and for pioglitazone-containing medicines from Takeda Pharmaceutical, and confirmed a…
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REGULATORY
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