How to Audit a Third-Party Pharma Manufacturing Partner
Auditing third-party pharmaceutical manufacturing partners is critical for ensuring product quality, regulatory compliance, and patient safety. A comprehensive audit evaluates GMP adherence, quality systems, documentation practices, and facility conditions. This systematic approach helps identify risks, verify supplier capabilities, and maintain supply chain integrity while meeting FDA and international regulatory standards for pharmaceutical excellence.
Read Blog: https://medium.com/@medellasof....tgel/pharma-manufact
#medellasoftgel #pharmamanufacturing #thirdpartymanufacturing #contractmanufacturing #gmpcompliance #pharmaaudit #qualityassurance #regulatorycompliance #pharmaceuticalindustry #supplieraudit #cmo #cdmo #drugmanufacturing #pharmaquality #manufacturingexcellence #fdacompliance #pharmasupplychain #qualitycontrol #pharmabusiness #lifesciences #pharmapartnersretry
