Picture your team submerged in a 45-hour investigation of a cracked vial, root cause: a single chipped tray edge. Meanwhile, a critical bioreactor pressure spike drifts untouched in the queue. This mismatch between effort and impact isn’t just inefficient; it’s a symptom of a system begging for risk-prioritized triage. 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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