Lifecycle Approach to Process Validation
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Management of an Effective CAPA
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Use of QRM in Cleaning Validation
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Clean Room Environmental Monitoring and Contamination Control
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QbD in Biologics Drug Product Development and Manufacturing
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QRM based Commissioning and Qualification
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Challenges in Analytical Method Transfer
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How to Validate Computerized GxP Systems in the Life Sciences 11 08 16
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