How to Handle Deviations During Equipment Qualification
In GMP environments, deviations during equipment qualification are not only common—they’re expected. Whether you’re qualifying a photostability chamber or a humidity-controlled incubator, unexpected issues may arise during IQ, OQ, or PQ. What matters most is how well those deviations are documented, investigated, and resolved. This guide is tailored for global pharma professionals and outlines a…
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