The Ministry of Health, Labor and Welfare (MHLW) on February 14 ordered label revisions for Pfizer Japan’s psychoneurotic agent Atarax (hydroxyzine), and Chugai Pharmaceutical’s BRAF inhibitor Zelboraf (vemurafenib) for the addition of new adverse drug reactions (ADRs). In its notification…
To read the full story
Related Article
- PMDA Risk Communication Update for Atarax, Zelboraf
January 23, 2017
REGULATORY
- Japan Approves AbbVie’s Aquipta, Novo’s IcoSema, Pfizer’s Tukysa, and More
February 20, 2026
- Health Minister Signals Early March Approval for iPSC Products
February 20, 2026
- Takaichi Urges Public-Private Investment Push in Drug Discovery
February 20, 2026
- Two iPSC-Derived Products Now in Line for Conditional Approval
February 20, 2026
- PM Takaichi Keeps Cabinet Intact after Lower House Vote
February 18, 2026
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…





