Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Clears All Its Review Targets, Processed Relief Claims at Record Speed in FY2021
The Pharmaceuticals and Medical Devices Agency (PMDA) achieved all its review time targets for drugs, medical devices, and regenerative medicine products in FY2021, according to its report presented at its steering committee meeting on June 17. For priority drugs, the…
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REGULATORY
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