Is your internal QA team becoming overwhelmed by the document review for a new facility project?
When commissioning and qualification are outsourced but quality oversight isn’t, it can strain your team and slow down your timeline.
This week’s Cen Weekly talks about why temporary quality support for temporary projects is a smart strategy, and how to make it work with the right partner.
Has your company found an effective way to handle QA support during a major expansion?
CenPharma is a pharmaceutical consulting firm specializing in compliance, engineering and technical services. We specialize in designing and implementing systems in diverse areas such as method design, method transfer, quality compliance, quality assurance, inspection readiness, process validation, analytical method validation, equipment qualification, facility design, supplier qualification, environmental monitoring, quality management systems, learning management systems, materials management, auditing (hosting and conducting), compliance remediation, quality systems, investigation, root cause analysis, technical writing, change management, data integrity and quality control. Our team consists of experience pharmaceutical industry professionals with expertise in microbiology, engineering, compliance, system design and regulatory affairs.
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