We provide the configurable technical controls, validation supports and security features for processing electronic data in regulated and non-regulated environments.
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The most versatile image management system for preclinical digital pathology offers comprehensive features for regulated and non-regulated studies. Comply with 21 CFR Part 11 requirements using robust solutions for archival, auditing, reason-for-change tracking and IQ/OQ reporting and customized validation supports. With Pathcore supporting your quality assurance team’s requirements, pathologists can focus on the science and adopt whole slide imaging with ease.
