Digital SOP for vendor audits in eQMS, LIMS and MES Systems: Best Practices
Vendor audits serve as a critical mechanism for pharmaceutical companies to assess the quality and compliance of their external partners. These audits not only evaluate adherence to Good Manufacturing Practice (GMP) but also verify alignment with respective regulatory frameworks. A well-structured SOP enables quality assurance (QA) professionals to systematically conduct audits and document activities to demonstrate compliance during inspections.
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