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 to Build Shared Database of GMP Inspection Reports
The Pharmaceuticals and Medical Devices Agency (PMDA) has begun work to build a database of quality-related information that will enable prefectural authorities to share findings from their inspections of drug manufacturing facilities. The plan is to finalize the system’s requirements…
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