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 Jascayd, mNEXSPIKE, Zepbound OSA Use, Others
May 19, 2026
- Japan to List 1st Biosimilars for Xolair, Ranmark, Simponi on May 20
May 19, 2026
- Japan Provides Stockpiled Avigan to UK for Hantavirus Prevention
May 19, 2026
- 800 More Entities Seek War-Tied Supply Consultation as Future Anxiety Spreads
May 19, 2026
- Japan to Swiftly Consider Safety Measures over Tavneos: Minister
May 19, 2026
In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





