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 Eyes Multi-Year Funding to Secure MCMs: Takaichi
October 14, 2026
- Pharma Continues Reform Push at 2nd Public-Private Subgroup Meeting
October 13, 2026
- AbbVie’s TrenibotE Up for Review on Oct. 26, Aquipta on Agenda Too
October 13, 2026
- Japan Panel to Review Full Approval of Nipro’s Stemirac on October 15
October 13, 2026
- Japan Finalizes Medical Data Sharing Blueprint, Eyes 2027 Bill
October 13, 2026
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…





