Nov 26Uh Oh…A Deviation On A GMP Batch - Now What?Deviation investigations are integral to continuous quality improvement, helping to eliminate recurrence in future production.
Oct 24Leveraging CDMO Expertise to Drive Sponsor Innovation and EfficiencyIn the fast-paced world of biopharmaceutical manufacturing, CDMOs play a critical role in facilitating...
Aug 22 Let's Get Critical!The main aspects of a critical reagent program include defined protocols for sourcing, qualification, stability monitoring, and resupply.