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 Accept All Requests for Generic Drug Face-to-Face Consultations
The Pharmaceuticals and Medical Devices Agency (PMDA) began accepting all requests for face-to-face consultations on generic products, following the creation of a new office to specifically review generic drugs. The PMDA accepted all five requests filed this month for January…
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REGULATORY
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