Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA’s Review-Related Ordinary Loss Nearly Doubled in FY2016
The Pharmaceuticals and Medical Devices Agency (PMDA) announced on June 26 at its steering committee meeting that the ordinary loss related to its review division nearly doubled to 1,888 million yen in FY2016. The division’s ordinary loss was 585 million…
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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…