Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA to Specify Target Overall Review Period for Regenerative Medicine Products: FY2019-2023 Plan
The Pharmaceuticals and Medical Devices Agency (PMDA) on January 16 presented a draft of its fourth midterm plan for FY2019-2023, newly setting the target total review time for regenerative medicine products. The agency aims to achieve a total review time…
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