The Japanese government on March 7 announced new NHI prices for the FY2025 drug price revision, effective April 1. With…
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PMDA Reviewing New Safety Risks for Soliris, Venclexta/Noxafil
The Pharmaceuticals and Medical Devices Agency (PMDA) is investigating new side effect risks for Alexion Pharmaceuticals’ C5 complement inhibitor Soliris (eculizumab), a move likely to trigger label changes in the near future. According to the agency’s risk communication update on…
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A Japanese health ministry panel on December 26 wrapped up its discussions on the next amendment of the Pharmaceuticals and…
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A Japanese health ministry panel discussing the generic industry structure on May 22 put together a report in which it…
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Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…
The Japanese health ministry’s expert panel tasked to discuss comprehensive policies for the rapid and stable supply of pharmaceuticals generally…