Vista LIMS delivers an intuitive, secure, and end-to-end ecosystem for sample handling, regulatory compliance, and intelligent laboratory automation.
Explore Full ERP FeaturesEnd-to-end tracking from Sample Collection to Final Disposal with full chain-of-custody.
Pre-configured for NABL accreditation and ISO/IEC 17025:2017 global compliance standards.
Leverage Artificial Intelligence to identify out-of-trend results and data entry errors automatically.
Strictly compliant with FDA 21 CFR Part 11, featuring electronic signatures and unalterable audit trails.
Direct equipment interfacing with HPLC, GC, and Spectrometers to eliminate manual transcription.
Real-time tracking of reagents and consumables with automated expiry alerts and reorder levels.
Centralized Master Data control for parameters, methods, and customer-specific specifications.
Design Customizable Reports for BIS, FSSAI, and private clients with dynamic digital signatures.
Seamlessly manage multiple lab branches from a single centralized headquarters dashboard.
A modern, easy-to-use UI reduces training time and ensures high adoption across all lab staff roles.
Prevent testing on uncalibrated devices with integrated preventive maintenance scheduling.
Adapt the workflow engine to match your specific laboratory SOPs and approval hierarchies.
Vista LIMS is an enterprise-grade Laboratory Information Management System (LIMS) built on a highly secure architecture. By integrating Master Data Management with real-time inventory control and equipment management, we provide a 360-degree view of your laboratory's efficiency. Our multi-location support ensures that global enterprises can standardize their testing protocols while maintaining ISO 17025 and NABL compliance at every branch.
With AI-driven insights and bidirectional instrument integration, Vista LIMS eliminates transcription errors and reduces turnaround time (TAT). Every report generated is fully customizable, allowing you to meet the specific branding and technical requirements of your customers while maintaining the highest levels of data security and access control.
Yes, Vista LIMS is specifically designed to meet NABL accreditation requirements and ISO/IEC 17025:2017 standards, providing full traceability for all testing activities.
Our AI-enabled engine monitors incoming test data in real-time, comparing it against historical trends and defined limits to flag potential outliers or "Out of Specification" (OOS) results instantly.
Absolutely. Vista LIMS supports automated equipment integration through bi-directional interfacing, allowing data to flow directly from the instrument into the LIMS without manual intervention.
Yes, for pharmaceutical and clinical labs, we provide a 21 CFR Part 11 compliant environment featuring electronic signatures, complex password policies, and comprehensive audit trails.
Yes, Vista LIMS is built for the enterprise. You can manage multiple lab locations from a single cloud-based instance with centralized Master Management and decentralized operations.
Yes, the workflow engine is highly customizable. You can define unique steps for Sample Receiving, Section Intake, Testing, Review, and Approval based on your lab's specific SOPs.
The integrated inventory module tracks reagents and consumables at the lot level. It can be set to automatically deduct stock as tests are performed and alert you when items reach a low-stock threshold.
Yes, Vista LIMS features a powerful reporting engine that allows you to create customizable report templates with dynamic branding, QR codes, and regulatory logos.
Yes, Vista LIMS is known for its intuitive and easy-to-use interface. The UI is designed to minimize clicks and streamline data entry, ensuring high user adoption across all technical roles.
Yes, Vista LIMS is a secure, web-based platform that allows authorized users to access the lab data, review results, and approve reports from any location with an internet connection.