e-AUTO is a powerful platform designed to automate and streamline business processes and workflows across departments, functions, and enterprise systems. Leveraging advanced logic and AI-driven task management, e-AUTO enables organizations to digitize manual operations, enforce structured workflows, and gain real-time visibility into every step of the process. It transforms repetitive, error-prone activities into controlled, auditable, and efficient workflows.

e-CFR is a dedicated regulatory compliance management system built to help organizations manage, monitor, and maintain adherence to the U.S. Code of Federal Regulations (CFR). Designed for industries subject to FDA, OSHA, EPA, and other federal oversight, e-CFR enables full lifecycle control of regulatory clauses, audit findings, gap analyses, and implementation tracking—ensuring real-time readiness, transparency, and accountability across the organization.

e-DHR is a robust Device History Records (DHR) management system designed for organizations that require meticulous documentation of manufacturing processes. Built with AI-driven automation, e-DHR streamlines the creation, management, and compliance of DHRs, ensuring product quality, regulatory adherence, and operational efficiency. It is an ideal solution for industries such as medical devices, electronics, and aerospace, where precise manufacturing records are critical.

e-DMR is a next-generation Device Master Record (DMR) management system engineered to support regulatory compliance, product quality, and manufacturing consistency. Designed for industries such as medical devices, electronics, and aerospace, e-DMR ensures that every product’s design, manufacturing, and inspection requirements are documented, maintained, and easily accessible. With built-in AI capabilities, e-DMR automates key processes, reduces manual overhead, and provides complete control over master documentation throughout the product lifecycle.

e-DHF is an advanced Design History File (DHF) management system tailored for organizations involved in product development and manufacturing, particularly in regulated industries such as medical devices. The system leverages AI technology to automate, streamline, and ensure compliance throughout the design and development lifecycle, making it easier to manage complex regulatory requirements and maintain thorough documentation.

e-DHF is the ultimate solution for organizations looking to manage their Design History Files efficiently, ensuring compliance, enhancing productivity, and improving control over the product design and development lifecycle.

e-GDPR is a comprehensive compliance management system designed to help organizations implement, manage, and monitor General Data Protection Regulation (GDPR) requirements effectively. Built with automation and security at its core, e-GDPR centralizes data protection policies, records of processing activities (RoPA), consent tracking, risk assessments, incident response, and regulatory reporting—all within one structured platform.

e-QMS is a comprehensive quality management system designed to centralize and automate the documentation, control, and execution of quality processes across the organization. Developed to support ISO 9001:2015 standards and other regulatory frameworks, e-QMS ensures full traceability, compliance, and continuous improvement by managing procedures, controlled documents, training records, customer complaints, audits, and more through a task-driven platform.