Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Beats FY2016 Review Time Targets
The Pharmaceuticals and Medical Devices Agency (PMDA) has cleared its FY2016 targets for shortening the total review time of new drugs - both for products in the standard and priority review pathways, the agency said on June 15. The total…
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