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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PMDA to Accept Regulatory Officials from KFDA for Training
At a symposium held on October 4 to commemorate the establishment of the Society for Regulatory Science of Medical Products, Toshiyoshi Tominaga, director of the PMDA's Office of International Programs, revealed that the PMDA will start accepting regulatory trainees from…
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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…