Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Plans Manufacturing Inspections for 2 Regenerative Medicine Products This Year
The Pharmaceuticals and Medical Devices Agency (PMDA) plans to conduct manufacturing practice inspections by the end of this year for two regenerative medicine products filed for approval under the Pharmaceuticals and Medical Devices Law, a PMDA official said on February…
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Conditional, Time-Limited Approval条件・期限付き承認January 29, 2015
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