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Global Compliance Panal
Manufacturing
Risk Analysis in Pharmaceutical Manufacturing A Regulatory OverviewGlobal CompliancePanel Webinar Areas Covered in the Session: * What are the regulatory guidance documents that relate to risk analysis? * What to do at really early stages of product development. * Hazard Analysis * Software problems? * What are the contributors to the hazards? Fault tree Analysis (FTA) * Evaluating Critical Failures. Failure Mode effect Analysis (FMEA) * Assessing Risk Severity * Risk Mitigation or Prevention * Choosing the assessment team |
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