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Created by: Matthew Jackson, Validation Manager, Torbay PharmaceuticalsThis article was based on my session, Cleaning Validation Program Design: Risk-based Lifecycle Approach, delivered at the KENX’s Cleanroom Validation, Disinfection & Environmental Monitoring Conference April 27-29, 2022 Virtually and in person in Philadelphia, PA.KENX’s hybrid conferences highlight those paving the way in best practices in cleanroom qualification, […]
Created by: Fred Ohsiek, Senior Global Technical Manager, Life Science (Cleaning Validation) for Ecolab in North AmericaDeveloping an automated clean-in-place (CIP) recipe is a challenging activity for project such as a new facility, equipment or wing addition to an existing facility, a new product, or optimizing a legacy cleaning process. This article will focus on […]
Created by: Leslie Lighton-Humphreys, ISO IT CSV & QA Manager, AmerisourceBergenLighton-Humphreys-Leslie_Mock-CSV-Audit-Workflow_Takeaway_Part-1Download
Created by: Scott Cady, Senior IT Quality & Compliance Consultant, Azzur GroupCady-Scott_Data-Integrity-Computer-Software-Assurance-Aligned-Framework-ModelDownload
Created by: Elizabeth Brockson, Associate Director, Global Quality Control, CAILiz_Brockson_EM-Trend-Evaluation-ToolDownload
