Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Launches Advisory Program for Academia, Startups Developing New Modalities
The Pharmaceuticals and Medical Devices Agency (PMDA) said on July 24 that it has launched a new regulatory consultation program designed to help academia and domestic startups commercialize innovative, Japan-origin drug candidates using novel modalities. Under the new program, the…
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REGULATORY
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