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
- MHLW Lifts Part of Approval Conditions for Takeda’s Vyvanse
June 9, 2026
- Drug Makers Seek Govt Support for Immunoglobulin Plant Investments: LDP Hearing
June 9, 2026
- Japan Govt Likely to Slim Down Honebuto, but Details Remain Elusive
June 8, 2026
- Leqembi, Kisunla Labels Revised to Strengthen ARIA Monitoring
June 8, 2026
- Japan Tightens Oversight of Mounjaro Resales: Health Minister
June 8, 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…





