Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA to Make Public Adverse Reactions Reported by Patients by Year-End
The Pharmaceuticals and Medical Devices Agency (PMDA) is set to revamp a trial service to accept adverse reaction reports from patients in preparation for its full launch, planning to make public the reported side effects by the end of the…
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REGULATORY
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