REGULATORY
Panelists Wary of Proposed Switch of Generic GMP Inspection Authority to PMDA
The Ministry of Health, Labor and Welfare (MHLW) on July 5 floated a legal change that would switch the authority to conduct GMP inspections for certain generic medicines from prefectural governments to the Pharmaceuticals and Medical Devices Agency (PMDA). The…
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…





