Checklist for Requalification After Equipment Changes
In a GMP-regulated pharmaceutical facility, equipment validation is not a one-time task. Regulatory bodies expect requalification after certain changes to ensure ongoing fitness-for-purpose. This checklist-style guide provides global pharma professionals with a complete breakdown of what must be considered when requalifying equipment—especially in stability testing contexts—after planned or unplanned changes. When Is Equipment Requalification Required?…
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