Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Beating Targets for Overall Review Time in FY2015
The Pharmaceuticals and Medical Devices Agency (PMDA) reported at a meeting of its committee on review and safety operations on December 16 that 60% of new drugs (priority products) were reviewed within 8.7 months in FY2015 (as of October 31),…
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REGULATORY
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Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…