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