Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PFSB Issues Notification on Marketing Authorization Applications for In Vitro Companion Diagnostics
The Office of Medical Devices Evaluation of the Pharmaceutical and Food Safety Bureau’s (PFSB) Evaluation and Licensing Division issued a notification on February 26 to prefectures regarding matters to keep in mind when submitting applications for the marketing authorization of…
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REGULATORY
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