REGULATORY

Japan Likely to Take FDA’s Anticipated EUA as Cue for “Special” Remdesivir OK

May 1, 2020
As overseas media reports the FDA’s emergency use authorization (EUA) for remdesivir is imminent following positive COVID-19 data, the Japanese government believes that such nod will constitute legal grounds for giving its “special approval” for the Gilead Science medicine, according…

To read the full story

Related Article

REGULATORY

Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…

By Hayate Horiguchi

Japan has entered a third straight year of wage hikes averaging 5%, but the pharmaceutical industry is struggling to keep…

By Philip Carrigan

We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…

Japan’s Central Social Insurance Medical Council (Chuikyo) on November 5 approved the reimbursement listing for a slate of new medicines,…

By Ken Yoshino

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…