The government should alleviate companies’ post-marketing regulatory burdens for intractable disease treatments if it is to encourage their development, a representative of the Japan Pharmaceutical Manufacturers Association (JPMA) told a health ministry panel on April 21. Osamu Inagaki, head of…
To read the full story
Related Article
- AMED Chief Envisages Tapping Private Funds to Fuel R&D
April 22, 2015
REGULATORY
- MHLW Issues Q&A on Conditional Approval System
May 1, 2026
- Panel Backs Proposal to Allow Antibody Drugs Like Beyfortus in NIP
May 1, 2026
- METI Clarifies Naphtha Comments, Reaffirms Medical Priority
April 30, 2026
- Japan Minister Rules Out Full Self-Pay for OTC-Like Drugs
April 30, 2026
- Govt’s Bio-WG Wraps Up Biopharma Investment Roadmap Draft
April 30, 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…





