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 Expand Consultation Services for Clinical Trials Initiated by Academia
The Pharmaceuticals and Medical Devices Agency (PMDA) will expand its consulting services by providing a “regulatory strategy consultation” service to academic institutions conducting late PII and subsequent exploratory clinical trials. This consultation service will be provided on a trial basis.…
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REGULATORY
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