ZyLAB announced the availability of its new FDA-compliant content-management solution for the pharmaceutical and biotechnology industries. 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. This ZyIMAGE solution 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 the ZyIMAGE solution 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. Full documentation has been prepared and approved for the ZyIMAGE solution. http://www.zylab.com