REGULATORY
Pharma Regulation Panel to Explore Potential Criteria for All-Case PMS Requirement
A health ministry study group on pharmaceutical regulations on January 12 discussed issues around the current post-marketing surveillance (PMS) scheme in Japan, including all-case PMS. With all-case PMS quite often required for newly approved medicines, the panel is set to…
To read the full story
Related Article
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…





