Analysis of individual placements across 43 companies over the past 18 months paints a vivid picture of Japan’s evolving healthcare industry. This comprehensive snapshot illuminates current market demands, strategic shifts, and the enduring appeal of this pivotal Asian market.Rare Diseases…
REGULATORY
Need of Placebo-Controlled Studies Will Be Decided on Case-by-Case Basis: PMDA Official
Case-by-case decisions will be necessary for clinical trials regarding whether placebo-controlled designs should be adopted or not as it is difficult to set universal guidelines, an official of the Pharmaceuticals and Medical Devices Agency (PMDA) said on January 19. Yumiko…
To read the full story
Related Article
REGULATORY
- Japan Panel to Review Kyowa Kirin’s Libmeldy for Approval on Nov. 9
November 4, 2026
- PMDA Sets Out AI Principles for Regulatory Activities, Stresses Human Oversight
November 4, 2026
- Public-Private Pharma Talks Expand to Domestic R&D, Manufacturing Investment
November 2, 2026
- Japan’s Healthcare Spending Hits Record 48.8 Trillion Yen in FY2024
November 2, 2026
- PMDA Renews Warning on Off-Label GLP-1 Use amid Adverse Event Reports
November 2, 2026





