Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Establishes Office of Generic Drugs to Expedite Review and Consultation for Generic Drugs
The Pharmaceuticals and Medical Devices Agency (PMDA) established a new office of generic drugs on November 1. By creating a separate office to review generic drugs, which up to now has been the responsibility of the Office of OTC/Generic Drugs,…
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REGULATORY
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