REGULATORY
PMDA’s Next 5-Year Plan to Embrace New Generic Unit, Benchmarks for Review Time
The Pharmaceuticals and Medical Devices Agency (PMDA) intends to stipulate the establishment of a generic review unit and targets for the overall review time for generics and new drugs in its next five-year plan starting in April. A draft for…
To read the full story
Related Article
- PMDA Looks to New Pre-Application Meetings to Shed Review Time
November 14, 2014
REGULATORY
- Japan Panel to Review Sumitomo, Cuorips iPSC Products on Feb. 19
February 16, 2026
- Update: DMD Gene Therapy Elevidys Cleared for NHI Listing at 305 Million Yen
February 13, 2026
- MHLW Orders Label Revisions for Vyxeos, Inlyta, Imbruvica, and More Drugs
February 13, 2026
- MHLW Orders Label Revisions for Sulfite-Containing Medical Products
February 13, 2026
- PMDA Urges Proper Use of Colchicine, Advises against High-Dose Administration
February 12, 2026
The Japanese healthcare sector is experiencing rapid growth, demanding a highly skilled and diverse workforce. However, finding and attracting the best talent in this competitive market presents significant challenges.Enter AI. With the rise of AI-powered tools, healthcare organizations can revolutionize…





