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Manufacturing Facilities
Pharma
Sanofi unit in Ireland dinged by FDA on Altuviiio production
After a site visit by FDA inspectors yielded a Form 483 for Genzyme in early 2026, the Sanofi unit is facing further scrutiny from the regulator.
Fraiser Kansteiner
Jul 1, 2026 2:52pm
Lilly, Regeneron among 7 chosen for FDA PreCheck Pilot Program
Jun 30, 2026 9:57am
Eisai gets UK backing as it expands plant for Leqembi production
Jun 15, 2026 10:20am
FDA unveils 1-day assessment pilot to complement inspections
May 6, 2026 3:08pm
Amgen adds $300M to US investment plan, targeting Puerto Rico
May 4, 2026 9:00am
FDA clarifies Form 483 expectations after production inspections
May 1, 2026 10:52am
