Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) on February 20 updated its list of drug safety risks currently under evaluation, flagging four categories of potential drug-drug interactions — a development that could lead to broad label revisions. Among the combinations…
To read the full story
Related Article
REGULATORY
- Zepbound in Line for OSA Approval after Key Panel Nod
April 27, 2026
- War-Linked Supply Concerns Rise to 43 Cases, Focus Shifts to Solvents, Packaging
April 24, 2026
- JPMA Pushes for “Freeze” on On-Patent Drug Price Cuts at LDP Meeting
April 23, 2026
- MHLW to Exclude High School-Age and Younger from OTC-Like Drug Charge: Official
April 23, 2026
- Japan, Singapore to Share GMP Inspection Results under Cooperation Pact
April 23, 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…





