Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Begins Disclosing Information on ADRs Reported by Patients through Online Patient ADR Reporting System
The Pharmaceuticals and Medical Devices Agency (PMDA) began on February 26 disclosing information on adverse drug reactions (ADRs) reported by patients (and their families) through its patient ADR reporting system, which is currently being operated online on a trial basis.…
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