Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Cabinet OKs PMDA’s Review Fee Raise from April 1
The Japanese Cabinet on March 24 approved a plan to raise the Pharmaceuticals and Medical Devices Agency’s (PMDA) review fees for drugs, medical devices, and regenerative medicine-based products, as well as GMP inspection fees, which will take effect in FY2017.Subject…
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