3iVerify is a comprehensive quality management software tailored for the pharmaceutical, biotech, and medical devices industries to automate compliance with regulatory standards like FDA's 21 CFR Part 11 and EU Annex 11. It includes features such as electronic recordkeeping, electronic signatures, RBAC for access control, and tools to manage documentation creation, approval workflows, training records, NCRs (Non-Conformance Reports), CAPAs (Corrective and Preventive Actions), audits, and change control processes. The software also offers real-time monitoring of data integrity and analytics to track performance indicators related to quality metrics.
3iVerify differentiates itself in the market through its specialized focus on automating compliance with stringent industry regulations. Its robust suite of tools supports extensive quality management activities while ensuring adherence to regulatory standards. Key features like real-time data monitoring and role-based access control further enhance its utility by providing comprehensive solutions for maintaining data integrity and tracking quality metrics efficiently within regulated environments.
In a competitive landscape that includes platforms like MasterControl, TrackWise, Veeva QualityOne, Sparta Systems, and EtQ Reliance; 3iVerify stands out due to its advanced capabilities in documentation management, workflow automation, NCRs/CAPAs handling, audit management along with real-time data integrity monitoring. These functionalities make it an appealing choice for professionals involved in quality management and regulatory affairs in highly regulated sectors seeking an efficient system that streamlines compliance processes while maintaining high-quality standards.
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