The process-oriented design of the arivis5D Compliance goes beyond electronic quality management with documents. The platform serves the needs of a well-regulated industry. With the whole Pharma life-cycle in mind the arivis5D Compliance platform has been designed with applications for well-known end-to-end processes and specifically closing the gaps in CAPA Monitoring, Change Control, Customer Complaints, Deviation Analysis, Vendor Qualification, Compliance Analysis, OOS / OOT, Record Management, and Training Management. The beauty of the platform approach comes in when customers need to blend in applications with existing systems and infrastructure, the platform creates value smart decision support and monitoring capabilities. arivis5D Compliance is made for seamless integration and combines ease-of-use with smart decision-making capabilities.
Scheduling enable the organizations to manage internal and internal audits. Mapping and tracking with CAPA items. Track progress and effectiveness
Administration and Monitoring modules
Completely integrate with quality systems
Integrates with SOP authoring process
Basing on a cloud-based platform, the reporting of quality metrics is effortless with patterns, dashboards, and KPIs
With arivis training services implementations are ready for success. The arivis5D Learning Management System (LMS) typically handles the processes related to ramp-up and adoption planning after larger implementations.