Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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PMDA Plans to Introduce Full Scale “Patient ADR Reporting System” by FY2018
The Pharmaceuticals and Medical Devices Agency (PMDA) plans to introduce a full-scale system for receiving reports of adverse drug reactions (ADRs) directly from patients by FY2018, the final year of its third midterm plan. A patient ADR reporting system was…
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