REGULATORY
Japan Set to Push Central IRBs for Clinical Trials, Avoid Customary All-Case PMS
A Japanese health ministry study group focused on pharmaceutical regulations on March 21 agreed on a policy to encourage the use of central institutional review boards (IRBs) in a bid to boost the efficiency of clinical trials in Japan. The…
To read the full story
Related Article
- MHLW Sets Exceptions to All-Case PMS through Revised Q&A
July 22, 2024
- Regulation Panel’s Final Report Specifies Exemptions for All-Case PMS
April 25, 2024
- Pharma Regulation Panel Wraps Up Debate, Report to Be Finalized Soon
March 22, 2024
- Pharma Regulation Panel to Explore Potential Criteria for All-Case PMS Requirement
January 15, 2024
REGULATORY
- 874 Defects or Health Damages Reported for Regenerative Medical Products in 1H FY2025
March 13, 2026
- Chuikyo OKs Listing of J&J’s Rybrofaz, Peak Sales Seen at 43.8 Billion Yen
March 12, 2026
- GSK’s Exdensur, Lilly’s Inluriyo Missing from March Listing Roster
March 12, 2026
- Truqap Price Cut Set at 10.7% from June under CEA Scheme
March 12, 2026
- Avelox Gains Coverage for MDR-TB via Public Knowledge Filing
March 12, 2026
I recently sat down with one of the leading medical directors in Japan to discuss the critical evolution of the medical science liaison (MSL) role.The MSL has transformed from a scientific resource into a strategic partner essential for successful product…





