Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Japan Approves 116 NMEs in FY2015, 37 on Priority Path: PMDA
The Pharmaceuticals and Medical Devices Agency (PMDA) said on August 18 that it achieved approval of 116 new molecular entities (NMEs) in the year ended March 2016, including 37 through priority review.The number of ethical drug products, counted based on…
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REGULATORY
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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…