Empower Your Quality Control with Automated Solutions

AmpleLogic OOT Management Solution

AmpleLogic OOT Software is a comprehensive solution designed to streamline the management of out-of-trend (OOT) results in quality control laboratories. It offers automated reporting, rapid investigation workflows, and seamless integration with existing quality systems, ensuring compliance with regulatory standards and efficient resolution of quality issues.

Efficiency, Compliance, Integration: Key Features

Automated Reporting-01

Automated Reporting

Streamline OOT reporting process with automated data collection and reporting functionalities.

Rapid Investigations-01

Rapid Investigations

Accelerate root cause analysis through predefined investigation workflows and automated task assignments.

Seamless Integration-01

Seamless Integration

Integrate with existing quality management systems for seamless data exchange and workflow coordination.

Compliance Assurance-01

Compliance Assurance

Ensure adherence to regulatory standards such as FDA guidelines and 21 CFR Part 11 through built-in compliance checks and audit trails.

Customizable Workflows-01

Customizable Workflows

Tailor workflows to fit specific organizational needs and processes for enhanced flexibility and efficiency.

Real-time Monitoring

Real-time Monitoring

Monitor OOT status and progress in real-time, enabling proactive management and timely interventions.

Automated Alerts

Automated Alerts & Notifications

Receive automatic alerts and notifications for pending tasks, approaching deadlines, and critical issues, ensuring timely action.

Configurable Dashboards

Configurable Dashboards

Create customizable dashboards to visualize OOT trends, metrics, and key performance indicators for informed decision-making.

Document Management-01

Document Management

Centralize document storage and retrieval, ensuring easy access to relevant information during investigations and audits.


Collaborative Platform

Facilitate collaboration among team members by providing a centralized platform for communication, document sharing, and task coordination.

OOT Management Simplified

Streamlined processes and automated workflows reduce manual effort and minimize the time required for OOT investigations, leading to increased productivity and faster resolution of quality issues.

Real-time monitoring and automated alerts enable proactive management of OOT situations, allowing organizations to address issues promptly before they escalate into larger problems.

Access to comprehensive OOT data and customizable dashboards enables informed decision-making based on real-time insights and trends, facilitating continuous improvement initiatives.

Integration with existing quality management systems and document repositories promotes data integrity and ensures a seamless flow of information across the organization, minimizing data silos and improving collaboration.

By reducing manual effort, minimizing errors, and optimizing resource allocation, OOT software helps organizations achieve cost savings in terms of time, labor, and potential product recalls or regulatory fines.

OOT software supports a culture of continuous improvement by facilitating root cause analysis, corrective and preventive actions (CAPA), and post-implementation reviews, driving ongoing optimization of quality control processes.

Frequently Asked Questions

It’s an automated solution for managing out-of-trend results in quality control labs.

By automating reporting, alerts, and integrating with other quality systems.

Yes, it adheres to FDA guidelines and other regulatory standards.

Absolutely, it offers configurable workflows and customizable reports.

Pharmaceutical, biotech, medical devices, chemicals, and more.

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