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 Lays Out AI Action Plan, Eyes Specialized In-House System
Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) has released an agency-wide action plan to expand the use of AI across its operations, outlining steps toward developing a proprietary AI system designed for its specialized regulatory work. The plan, finalized on…
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Strategic Talent Acquisition in the Japanese Life Sciences Sector: Your Market Intelligence Briefing
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Japan’s FY2026 drug price revision, officially announced on March 5, has landed poorly with the pharmaceutical industry — and the…
Japan’s Central Social Insurance Medical Council (Chuikyo) on November 5 approved the reimbursement listing for a slate of new medicines,…
The Japanese government on March 7 announced new NHI prices to be applied in the FY2025 drug price revision, revealing…
The Japanese government approved a bill to amend the Pharmaceuticals and Medical Devices (PMD) Act at its Cabinet meeting on…
Japan’s health ministry doled out regulatory approvals for a throng of new medicines on December 27 including Eli Lilly’s obesity…
Japan’s all-important reimbursement policy panel on December 20 approved an outline of drug pricing reforms for FY2024, which enshrines a…