When we think of audit preparation, our minds go to data integrity, protocol reviews, and staff readiness. But behind every smooth inspection lies a layer of often-overlooked details: the logistics. How you manage the practical elements, from the workspace to the workflow, can set the tone for the entire audit. A disorganized back-end can unintentionally signal a disorganized quality system, even if your technical compliance is perfect. Read More >
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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