Analysis of individual placements across 43 companies over the past 18 months paints a vivid picture of Japan’s evolving healthcare industry. This comprehensive snapshot illuminates current market demands, strategic shifts, and the enduring appeal of this pivotal Asian market.Rare Diseases…
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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