Behind every headline-making GMP failure lies a series of smaller, subtler choices, moments where professionals like you weigh risks, pressures, and principles in real time. These aren’t scenarios with clear right or wrong answers. They’re the gray zones where rulebooks fall short, and judgment becomes your most critical tool. This week, we explore four situations that test not just your knowledge of compliance, but your courage to uphold it. 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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