Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Dr Hayakawa Calls For Flexible Applications of Guidance on Biosimilars
At a seminar for regulatory affairs experts sponsored by the Society of Japanese Pharmacopoeia (SJP) on September 30, Takao Hayakawa, special advisor to the PMDA (Pharmaceuticals and Medical Devices Agency) and director of the Kinki University Pharmaceutical Research and Technology…
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Japan’s pharmaceutical industry is undergoing a structural shift in its workforce, with the role of sales reps shrinking while production…
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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…