Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Testing New System that Uses Electronic Medical Information to Help Assess Post-Marketing Drug Risk
The Pharmaceuticals and Medical Devices Agency (PMDA) has started a “MIHARI (Medical Information for Risk Assessment Initiative) Project” to test new post-marketing safety measures. The project is testing a new system for secondary use of electronic medical information such as…
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