Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Applications for “Regulatory Strategy Consultation” Increasing Rapidly: Mr Isobe of PMDA
As of November 1, the Pharmaceuticals and Medical Devices Agency (PMDA) had received a total of 67 applications for interviews preparatory to “regulatory strategy consultation,” a service it introduced on July 1. The service is designed to encourage the development…
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REGULATORY
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March 6, 2026
- Japan's Revised Drug Distribution Guidelines Take Effect
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- Japan Drug Prices to Fall 4% in FY2026 Revision: Official Gazette
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Japan’s FY2026 drug pricing reform will, for the first time, apply the “G1” price cut rule for long-listed original biologics…
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…
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…