Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
COMMENTARY
Will It Be Possible to Eliminate Unnecessary Equivalence Studies for Generics?
Some generic manufacturers supply healthcare providers with bioequivalence data, which compare drug concentrations in the blood, on generics administered through the intravenous route such as anticancer drugs although such data are not required by the national guidelines. They do so…
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COMMENTARY
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