Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Reviewing Safety Risks for GLP-1 Agents
The Pharmaceuticals and Medical Devices Agency (PMDA) is investigating new side effect risks of cholecystitis, cholangitis, and cholestatic jaundice for a slew of GLP-1 receptor agonists, a move likely to trigger label changes in the near future. Subject to the…
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