Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Building “Database on Unapproved Drugs” to Accelerate Elimination of Drug Lag
The Pharmaceuticals and Medical Devices Agency (PMDA) outlined its project plan for FY2013 at a meeting of its Review and Safety Committee on June 14. The agency reported that it is building a “Database on Unapproved Drugs” (tentative) to accelerate…
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REGULATORY
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