Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
MHLW Urges Generic Drug Makers to Ensure Availability of Products for All Indications Approved for Original Drugs
The Health Policy Bureau’s Economic Affairs Division and the Pharmaceutical and Food Safety Bureau’s Evaluation and Licensing Division issued a notification dated March 29 asking generic drug manufacturers to quickly address the problem of differences in indications between original drugs…
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REGULATORY
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