Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
PDUFA Date Set for Jan. 31, 2017 for Daiichi Sankyo’s Nausea Drug
Daiichi Sankyo said that the US FDA has accepted its new drug application for the nausea drug CL-108 it licensed from US pain specialty firm Charleston Laboratories, with a target action date under the Prescription Drug User Fee Act (PDUFA)…
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