Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
G-CSF Preparations under PMDA Review for Anaphylaxis
The Pharmaceuticals and Medical Devices Agency (PMDA) is reviewing the risk of anaphylaxis for G-CSF preparations including Gran (filgrastim) and its biosimilar versions - a move that is likely to result in label changes. Other G-CSF preparations under review are…
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