Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
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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