This eLearning video delivers a clear, well-designed overview of deviation management in pharma—explaining what deviations are, why they matter, and the key steps to identify, investigate, and close them for stronger GMP compliance.
This expertly designed eLearning video provides a clear, structured overview of deviation management in pharmaceutical environments. Built with strong instructional design, it explains what deviations are, why they matter under ICH Q10 and PQS expectations, and the essential steps for handling them—identification, documentation, investigation, evaluation, CAPA, and closure. The video helps learners understand how systematic deviation handling strengthens compliance, reduces recurrence, and supports continuous improvement across GMP processes.