Overview

The PCR.AI Device Manager provides a unified, web-based solution for managing all your PCR platforms and tests. Designed to integrate seamlessly with your laboratory workflow, it enables you to adjust tests and standard operating procedures (SOPs) for both sample-to-answer and laboratory-developed test (LDT) platforms within a single, powerful interface.

Key Features

Our Device Manager delivers comprehensive functionality to streamline your PCR operations:

Web-Based Platform Management

Access and control all your PCR platforms through a secure, browser-based interface from anywhere, ensuring consistent management across your entire laboratory network.

Advanced Data Management

Centralize and organize your test data with intelligent categorization, making it easy to track, analyze, and report on all PCR activities across multiple platforms.

LIMS Integration

Seamlessly connect with your existing Laboratory Information Management System (LIMS) to ensure smooth data flow and eliminate manual data entry errors.

Real-Time Platform Monitoring

Monitor the status and performance of all connected PCR platforms in real-time, enabling proactive maintenance and minimizing downtime.

Quality Assurance & Reporting

Generate comprehensive QA reports and periodic summaries to maintain compliance and track performance metrics across your testing operations.

Intelligent Alert System

Receive customizable alerts for critical events, maintenance requirements, and result anomalies, ensuring nothing falls through the cracks.

Test Modification Documentation

Maintain complete audit trails of all test modifications with detailed documentation, supporting regulatory compliance and quality control requirements.

Intended Usage

The PCR.AI Device Manager is specifically designed to assist qualified laboratory personnel in the management and review of PCR test results within clinical laboratory settings. The system enhances your workflow by:

  • Applying user-defined rules to automatically process results according to your laboratory’s specific protocols
  • Flagging results requiring human review to ensure critical findings receive appropriate attention
  • Supporting workflow and quality control processes through intelligent automation and tracking
  • Holding results for manual assessment when predefined criteria indicate the need for expert review

Technical Capabilities

The Device Manager is engineered to support modern molecular diagnostics workflows:

Flexible Rule Engine

Create and apply custom rules tailored to your laboratory’s specific requirements, ensuring consistent result interpretation across all platforms.

Comprehensive Curve Analysis

Designed for sample-to-answer tests, the system provides sophisticated curve analysis capabilities to support accurate result interpretation.

Modular Architecture

While the standard configuration does not include AI API integration, the system’s modular design allows for seamless addition of advanced capabilities:

  • CE-IVDR API integration available upon request
  • Custom module development to meet specific laboratory needs
  • Scalable architecture to grow with your testing volume

Implementation Benefits

By implementing the PCR.AI Device Manager, laboratories can expect:

  • Increased Efficiency: Reduce manual tasks and streamline workflows
  • Enhanced Quality: Improve consistency and reduce errors through automation
  • Better Compliance: Maintain comprehensive audit trails and documentation
  • Improved Visibility: Gain real-time insights into platform performance and test results
  • Scalable Operations: Easily manage growth in testing volume and platform diversity

Get Started

Ready to transform your PCR platform management? Contact our team to discuss how the PCR.AI Device Manager can be tailored to meet your laboratory’s specific needs. We offer:

  • Personalized demonstrations
  • Implementation planning assistance
  • Training and support programs
  • Custom configuration services
FAQ

Frequently Asked Questions

GENERAL PRODUCT QUESTIONS

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IMPLEMENTATION & TECHNICAL

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REGULATORY & VALIDATION

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Automated Analysis

Clinically proven accuracy
Reduced hand-on time
Faster results
Audit trails and metrics