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In-depth Insights of Tech Transformation
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Discover how digital pathology software that is fully integrated with LIMS addresses the most common requirements and concerns of pathologists working in leading pathology and preclinical diagnostic labs.
Discover how technology, software, and automated processes are modernizing effective compliance.
Learn how comprehensive SEND package preparation and review streamlines your SEND Submissions.
Learn the smarter path to managing the new digital lab environment.
Learn how to be effective in the new era of electronic quality management.
Learn more about the butterfly effect of COVID-19: A New Digital Paradigm for the post-COVID-19 World.
Learn how to sustain quality, compliance, and validation process after the initial steps.
Learn the solutions for common non-compliance issues in regulated labs.
Learn how to take an ROI based approach on managing compliance process and technology.
Learn the tools and techniques for managing absolute time compliance for electronic records, spreadsheets, files, and instrument outputs
Learn about how to take control of spreadsheets for 21 CFR Part 11 compliance with minimal system and operator changes.
Learn about the basic criteria and challenges for complying with e-source data management compliance.
Learn how to bring calibration, process and operating data for 21 CFR Part 11 compliance.
Learn how to ensure accuracy and compliance of data and the management processes.
Learn about the shifting EHS paradigm, how a quality digital EHS platform can impact the worker’s health and safety journey, and more.
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