Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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JMA’s New Pharma Affairs Exec Wants More Stringent Rules on Sakigake, Conditional Approval
Japan should tighten its drug reviews under the sakigake designation pathway and conditional early approval scheme, which will be revamped with solid legal backing in September under the amended Pharmaceuticals and Medical Devices (PMD) Law, Masaaki Miyakawa, who leads pharmaceutical…
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