The ZyIMAGE solution is used for digital capture and archiving of lifecycle GMP records, as well as all paper records requiring back up, such as validation protocols, validation reports and batch records. It also controls document review and access through a specialized interface or web browser, while maintaining a full audit trail of all actions performed. Customers are able to adapt and implement in departments across the firm, such as R&D, engineering, manufacturing, quality control, distribution, and global operations. In accordance with FDA guidelines, the audit trails utilized by this ZyIMAGE solution for relevant actions are fully compliant with 21 CFR Part 11. www.zylab.com
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