Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Evenity under PMDA Risk Review
The Pharmaceuticals and Medical Devices Agency (PMDA) is reviewing a new risk for Amgen Astellas BioPharma’s osteoporosis drug Evenity (romosozumab) - a move that is likely to result in label changes. The drug is being reviewed for risks associated with…
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