Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA’s Regulatory Consultation Service Off to Good Start, but More Effort Needed to Promote Face-to-Face Advisory Meetings: Dr Isobe
Soichiro Isobe, director of the Pharmaceuticals and Medical Devices Agency’s (PMDA) Office of Review Management, told Jiho in a recent interview that the results of the first year of the regulatory strategy consultation service, which started in July last year,…
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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…