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An Industry-Agnostic LIMS Solution

Qualis LIMS is a configurable Laboratory Information Management System (LIMS software) that unifies your lab operations into a secure, paperless, and compliant cloud-based environment—from sample receipt to final report delivery and beyond. Designed for industries where precision and regulation are critical, Qualis LIMS offers an intuitive way to manage samples, execute tests, automate workflows, and record results from a central secure platform.

Qualis LIMS provides integrated out-of-the-box modules that can be used by any QC, Research, Healthcare or Commercial lab. It provides a structured method to document laboratory investigations & results while adhering to various regulatory compliance requirements (21 CFR Part 11, EudraLex Annex 11, ISO 17025, GLP, GAMP 4)

higher productivity via automated workflows & reporting

30%

faster audit readiness due to full data traceability

40%

fewer transcription errors in data entry

40-60%

faster sample testing throughput

70%

Flexible Sample Registration & Testing

Register and test any sample type - raw materials, finished products, patient samples, clinical trial specimens, or R&D project samples
  • Dynamic sample registration templates with drag-and-drop fields .
  • Version-controlled template management for data integrity
  • Sample lifecycle tracking with complete metadata capture
lab report template

Beyond Basic Lab Management

Empowering Efficiency, Compliance, and Growth.

1
Sample Pre-Registration/ Registration
2
Result Entry (Manual, Instrument interface)
3
Approval & Release (HOD, Study Director, CRO)
4
Reports

Unified Test and Specification Management
  • Manage Test Groups

    Create and manage multiple test groups for samples based on Test Parameters.

  • Maintain Traceability

    Manage test specifications with Version control and release control

  • Define Test Specifications

    Set Limits based on expected test Results

biopharma
Live Dashboards & Alerts
  • Comprehensive Dashboard

    Real-time KPI dashboards for operational visibility

  • Intuitive Alerts

    Automated alerts for approvals, calibration due dates, job assignments, and non-conformance eventslity

  • Controlled View

    Customizable, role-based views for managers, analysts, and QA

biopharma
data collection instrument
Allocate Jobs to Certified Personnel & Qualified Instruments
  • Allot Jobs

    Allocate tests, instruments, and samples to be tested for various personnel.

  • Assign Role-Specific Tasks

    Allocate Role based tasks to lab personnel for performing specific tests.

  • Allocate Tests to Certified Personnel

    Ensure that certified personnel are allocated to specific jobs or techniques.

Import inventory Download LIMS Brochure
Standardized Inventory Management
  • Assign Barcode Labels

    Maintain Multiple Categories of Inventory Material with Barcode labeling

  • Track Inventory Levels

    Record and track usage of Inventory .

  • Optimize Material Storage

    Create Dynamic Storage Structures for Storing Materials

Import inventory See product in action
laboratory information management system
lims system software
Instrument & Equipment Management
  • Track Instruments Usage

    Maintain all instruments and equipment used across the laboratory

  • Maintain Instrument Logs

    Keep track of the Validation, Calibration and maintenance of instruments

  • Verify Instrument Reliability

    Ensure that only calibrated instruments can be assigned for tests.

Import inventory Download LIMS Brochure
Automated Result Entry & Reporting
  • Design Report Templates

    Design Templates for reports with Built-In Reporting Tool and auto-generate SQL Queries for reporting with Query Builder

  • Approve & Release

    Approve and Release reports in seconds with Electronic and digital signatures

  • External Report Access

    Make reports available for external stakeholders through Qualis Portal

Import inventory Explore Reporting & Qualis Portal
example lab report

Why Modern Labs choose Qualis LIMS

Web-based & platform-independent

Chrome, Firefox, Safari etc

Highly scalable

multi-site, multi-department, multi-lab

No-code configurability

tailor workflows without programming

Compliance-ready

21 CFR Part 11, EudraLex Annex 11, ISO 17025, GLP, GAMP 4

Lower cost of compliance 

pre-validated modules and audit-ready features

Industries & Use Cases

Pharmaceutical Quality Control & QA

Batch release, finished product testing, stability studies, CAPA tracking, deviation documentation, and compliance with data integrity standards such as 21 CFR Part 11 and EudraLex Annex 11

Healthcare & Clinical Diagnostics

Patient sample tracking with full chain-of-custody, integration across hospital and diagnostic networks, and improved testing throughput through automated data exchange and quality control traceability.

Life Sciences Research  

Centralized management of research data, sample metadata, and assay tracking enabling multi-site collaboration, version-controlled documentation, and reproducible experimental workflows

Food Safety & Quality Testing

Ingredient traceability, microbial and chemical QC testing, and compliance documentation aligned with regulatory and quality standards

Environmental & Water Testing Labs 

Field-to-lab sample management, monitoring of contaminants and water parameters, and adherence to local and international environmental regulatory standards

Chemical & Industrial Manufacturing

GLP-compliant QC testing, deviation and CAPA management, process validation, and data-driven optimization for continuous quality improvement

Compliance & Audit-Readiness

Designed with ALCOA+ principles, audit trails, role-based access control, and electronic record integrity. und elektronischer Datensatzintegrität. Qualis LIMS helps teams stay inspection-ready for  FDA, EMA, NABL, and ISO audits, minimizing preparation time and documentation effort.

Key Benefits at a Glance

Store sample
Complete Workflow Automation

from sample registration to report release

Store sample
Regulatory Compliance Built-In

21 CFR Part 11, ISO 17025, GLP, GAMP 4

Store sample
Enhanced Data Integrity

ALCOA+, secure audit trails, granular access

Store sample
Faster Turnaround Time (TAT) 

alerts, dashboards, high-throughput sample testing

Store sample
Scalable for Any Lab Size

single site to global multi-location

Store sample
Cost-Effective Deployment

SaaS or on-premise with low IT overhead

Deployment Flexibility

Deploy Qualis LIMS on AWS, Azure, customer-owned private cloud, or on-premises infrastructures

Deployment Flexibility

Deploy Qualis LIMS on AWS, Azure, customer-owned private cloud, or on-premises infrastructures

azure

Customer Success Snapshot

Global Healthcare Diagnostics Provider — Multi-Site Rollout

moderna covid vaccine
Challenge:

Manual sample tracking and fragmented reporting caused delays and compliance risk

Solution:

Deployed Qualis LIMS across 8 facilities with instrument connectivity, centralized dashboards, and barcode-enabled inventory.

Results:

Results: 40% faster TAT, 100% audit readiness within 3 months, and seamless cross-site collaboration.

Interested In Our Product Services?
Request A Demo Email US Contact Us

Frequently Asked Questions

A Laboratory Information Management System delivered via the cloud to manage samples, workflows, and compliance from any location. Learn about deployment options

Yes. It supports 21 CFR Part 11, ISO 17025, GLP, and GAMP 4 with e-signatures, audit trails, and secure access controls.
Download Compliance Datasheet

Yes. Qualis LIMS integrates with Logilab ELN, Logilab SDMS, and lab instruments via RS232/TCP/IP. Explore ELN Integration  or  SDMS Integration

Absolutely. Qualis LIMS scales from single-location labs to multi-site enterprises. Request a Demo to see a small-lab configuration

Would you like to learn more about Qualis LIMS?

Submit this form and our sales representative will contact you soon.
Email Us: [email protected]