BUSINESS

FDA Advisory Committee Recommends Approval of Rivaroxaban for SPAF

September 13, 2011
Bayer HealthCare of Germany has announced that the US FDA’s Cardiovascular and Renal Drugs Advisory Committee has recommended the approval of rivaroxaban (overseas brand name: Xarelto), an oral Factor Xa inhibitor, for stroke prevention in patients with atrial fibrillation (SPAF).…

To read the full story

BUSINESS

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

By Takashi Ebisawa

Japan’s plasma-derived product industry is approaching a turning point as the government prepares to step in with unprecedented support for…

By Philip Carrigan

The Wednesday TableShe had been on virtual calls since eight in the morning. The screen glowed. Her eyes burned. Plugged into Teams across time zones, she was digitally connected yet entirely isolated from the reality of Japan’s pharma market.She needed…

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…