Frequently Asked Questions

A LIMS or Laboratory Information Management System is a software solution that addresses the data management, automation, and regulatory challenges (ISO 17025:2017, FDA 21 CFR Part 11, CAP, etc.) of laboratories. LIMS is used to manage laboratory samples and the associated data effectively and efficiently, thus standardizing operations by automating process & workflows, managing tests, and handling reporting procedures. Overall, a LIMS enhances the efficiency, accuracy, and reliability of laboratory operations, supporting better decision-making and improved outcomes. With the growing needs of laboratories, the next-gen LIMS evolved, with the system being able to do much more than just tracking samples.

An ultimate next-gen LIMS solution for any laboratory which has to be AI Powered, no-code, process-based, and comprehensive laboratory information management system that is secure, reliable, and cost-effective solution to digitalize your complete laboratory and make compliance with ISO 17025:2017, FDA 21 CFR Part 11, CAP, etc. The next-gen LIMS (Laboratory Information Management System) digitalize and manage your entire laboratory data, workflows, quality, and compliance.

  • A no-code platform that allows users to configure and customize the system without any programming skills.
  • A process-based solution that adapts to the specific workflows and business rules of each laboratory.
  • A comprehensive suite of modules that covers all aspects of laboratory management, such as sample management, instrument integration, inventory management, stability study, document management, CAPA, audit management, competency management, task management, user management, SQC/SPC, custom reports, MIS dashboard, analytics, and complete audit trail.
  • A cloud-based or on-premise deployment option that suits the needs and preferences of each customer.

Implementing LIMS in your laboratory should be easy and fast with proven methodology and experienced team:

 
  • Requirement analysis:Need to understand your current processes, challenges, expectations, and future plans.
  • Solution design: Propose a suitable solution that meets your requirements and budget.
  • System configuration: Configure the system according to your specifications and preferences
  • System validation: Need to test the system to ensure its functionality and reliability once configured.
  • Data migration: Need to transfer your existing data to the new system with minimal disruption.
  • User training: Need to train your end-users to use the system effectively and efficiently.
  • Go-live support: Ongoing support and maintenance to ensure your satisfaction and success.

Yes, Revol LIMS is highly customizable to meet the specific needs of different laboratories, whether in testing, research, diagnostics, or manufacturing. You can tailor workflows, reports, and data management features based on your requirements.

Yes, Revol LIMS supports seamless integration with a wide range of laboratory instruments, allowing for automatic data capture and ensuring consistency and accuracy across your lab’s operations.

Yes, Revol LIMS is fully compliant with industry regulations such as ISO 17025 and FDA 21 CFR Part 11, ensuring your laboratory adheres to necessary standards for data integrity and security.

Revol LIMS employs industry-standard encryption, access controls, and regular backups to ensure your lab’s data is secure, protecting against unauthorized access and data loss.

Revol LIMS is designed with an intuitive interface to ensure ease of use for laboratory personnel, reducing the learning curve and improving efficiency.

Revol LIMS offers both cloud-based (PaaS/SaaS) and on-premise deployment options, giving you the flexibility to choose based on your lab’s infrastructure and preferences.

Yes, Revol LIMS is designed to be scalable and can accommodate the growing needs of your laboratory, whether you are adding more users, samples, or instruments.

Revol LIMS can support multi-location laboratories, providing centralized data management and ensuring consistency across all sites.