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ARTICLES
See the latest about BrevisRefero



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.
Nov 26, 2024


Leveraging CDMO Expertise to Drive Sponsor Innovation and Efficiency
In the fast-paced world of biopharmaceutical manufacturing, CDMOs play a critical role in facilitating...
Oct 24, 2024


Let's Get Critical!
The main aspects of a critical reagent program include defined protocols for sourcing, qualification, stability monitoring, and resupply.
Aug 22, 2024
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