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Risk Assessment in Pharma Practical FMEA & GMP Case Studies
Free Download Risk Assessment in Pharma Practical FMEA & GMP Case Studies
Published 12/2025
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Language: English | Duration: 2h 13m | Size: 1.47 GB
Learn practical FMEA, real GMP case studies, contamination risk control, mitigation, and data-driven decisions under ICH
What you'll learn
Learn how to identify failure modes, evaluate risks, and build an FMEA according to ICH Q9 principles.
Understand how to score Severity, Probability, Detectability and interpret RPN for objective decisions.
Apply risk assessment tools to real GMP case studies, including cleanroom flooding and gowning flow changes.
Develop practical QA skills: defining mitigations, linking them to CAPA/CC, and documenting decisions clearly.
Gain confidence performing risk assessments across manufacturing units: upstream, downstream, buffer prep, QC.
Requirements
Basic understanding of GMP processes is helpful, but not required. All concepts are explained clearly.
Description
Master practical Quality Risk Assessment in pharma using real GMP case studies, clear logic, and hands-on tools.This course is designed for QA, QC, Production, Validation, and Regulatory professionals who want to understand how to evaluate risks, prevent failures, and make objective, traceable decisions under ICH Q9.You will learn the full FMEA workflow step-by-step: how to define processes, identify failure modes, evaluate Severity-Probability-Detectability, calculate RPN, and determine which risks are acceptable, ALAP, or unacceptable. Throughout the course, we focus on practical application-not theory-using real GMP examples.A central part of this course is a real cleanroom flooding deviation case. You will analyze gowning flows, contamination risks, material movement challenges, environmental monitoring decisions, and mitigation strategies implemented across multiple manufacturing units. This case shows exactly how QA teams work during complex events.You will also practice linking mitigation actions to CAPA and Change Control, learn how to document risk assessments professionally, and understand how auditors expect decisions to be justified with objective evidence.By the end of the course, you will be able to perform risk assessments independently, support investigations, improve production reliability, and contribute to strong GMP compliance.This course is suitable for all levels, including beginners who want to enter the pharma QA world and experienced professionals who want to strengthen their practical risk management skills.
Who this course is for
For QA specialists, auditors, and validation engineers working with ICH Q9 and data-driven risk decisions.
For cleanroom operators, lab analysts, and manufacturing staff who need to understand risks and prevent failures.
For experienced GMP professionals seeking deeper skills in risk assessment, mitigation, and CAPA decision-making.
For beginners in pharma QA who want to learn FMEA, identify risks, and make objective GMP decisions.
Homepage
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