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 Introduce Direct ADR Reporting System for Patients on Trial Basis
Before the end of the current fiscal year ending in March, the Pharmaceuticals and Medical Devices Agency (PMDA) will begin testing a new adverse drug reaction (ADR) reporting system that will take reports of ADRs directly from patients. The PMDA…
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