Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
Meiji Seika’s Korean JV Passes GMP Inspection by PMDA, Preparing for Contract Production of Nesp Biosimilar
Meiji Seika Pharma said on September 26 that DM Bio, a joint venture with Dong-A Socio Holdings of South Korea, has passed a GMP compliance inspection for biopharmaceutical manufacturing by Japan’s Pharmaceuticals and Medical Devices Agency (PMDA). DM Bio is…
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