Wire · opportunities
Jubilant Pharmova's US facility Line 3 gets FDA nod for commercial production
◆ Sectors
Medtech
◆ Geography
United States
◆ Source
◆ Verified
Fusion42 · 24 August 2026 · Fusion42 review
Jubilant Pharmova's Spokane-based US facility received FDA approval for commercial batch manufacturing on its new Line 3, featuring an isolator-based fill and finish line with a capacity of 55 million units annually and advanced sterile injectable technologies.
This Wire brief sits within Fusion42's coverage of Medtech.
◆ ◆ The Wire takeaway
You can expand your US sterile injectable supply by partnering with a newly FDA-approved CDMO in Spokane, which means faster market access for liquid and lyophilized products.
◆ Coverage
1 source · 24 Aug 2026
◆ Related on Wire
◆ Topics
Medtechfda-approvalcommercial-productionsterile-injectablescdmopharma-manufacturing