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quality control
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
Fierce Biotech
Lilly debuts Nvidia supercomputer with fanfare and focus
Feb 27, 2026 1:37pm
Teva debuts innovation platform to parry key industry challenges
Nov 19, 2025 8:38am
Novo adds $112M quality testing lab to list of China investments
Jul 9, 2025 10:09am
FDA hits Piramal with 6-observation Form 483 at India API plant
Feb 26, 2025 10:22am
Sanofi hit with warning letter at Massachusetts ingredient plant
Jan 21, 2025 12:26pm