Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA’s New Mid-Term Plan to Push Pediatric, Orphan Drug Development to Counter Losses
The Pharmaceuticals and Medical Devices Agency’s (PMDA) new mid-term plan starting next April is expected to embrace numerous measures to stamp out drug losses including active support for the development of pediatric and orphan medicines, according to its outline. The…
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