Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
COMMENTARY
PMDA Sets Target Review Times for Partial Changes to Generic Approval - A New Way to Underpin Stable Supply
The Pharmaceuticals and Medical Devices Agency’s (PMDA) new five-year plan for FY2014-FY2018 sets targets for overall review time for partial modifications of approval for generics and long-listed products, or off-patent original drugs. The PMDA aims to reduce review time to…
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Japan is finally launching technical discussions on its cost-effectiveness assessment (CEA) system. A health ministry-funded research group is set to…
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