Ensure product quality, safety, and compliance with expert insights on Deviation Management in regulated industries. The AssurX Quality Management System (QMS) provides Life Sciences, Medical Device, and Manufacturing organizations with a unified platform to identify, document, investigate, and resolve deviations efficiently—reducing risk while maintaining full regulatory compliance.
Explore best practices and strategies for managing deviations in production and laboratory environments, integrating CAPA and root cause analysis, and meeting FDA 21 CFR Part 820, ISO 13485, and GMP requirements. Learn how automation, configurable workflows, and real-time analytics help streamline deviation reporting, improve traceability, and drive a culture of continuous improvement.
From minor process deviations to major nonconformances, discover how AssurX QMS enables organizations to detect early, act faster, and prevent recurrence—strengthening product integrity and regulatory confidence across the value chain.
