Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Applications Based on the Revised PAL to Be Accepted from Nov. 25
The Pharmaceuticals and Medical Devices Agency (PMDA) announced on its website on October 14 that it will accept marketing authorization applications and applications for GMP inspections based on the Pharmaceuticals and Medical Devices Law starting November 25. Since the three…
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REGULATORY
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