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Join date: Dec 17, 2021
Posts (11)

Nov 27, 2024 ∙ 5 min
Uh Oh…A Deviation On A GMP Batch - Now What?
Deviation investigations are integral to continuous quality improvement, helping to eliminate recurrence in future production.
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Oct 24, 2024 ∙ 4 min
Leveraging CDMO Expertise to Drive Sponsor Innovation and Efficiency
In the fast-paced world of biopharmaceutical manufacturing, CDMOs play a critical role in facilitating...
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Aug 23, 2024 ∙ 5 min
Let's Get Critical!
The main aspects of a critical reagent program include defined protocols for sourcing, qualification, stability monitoring, and resupply.
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brevisrefero
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