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Driven by regulatory compliance and having to ship products across the globe, it becomes all the more complex for the pharmaceutical industry to comply with the regulations of various countries.

Going digital is no more a luxury but a de-facto standard for the industry.

Qualis® LIMS (Laboratory Information Management System) from Agaram Technologies was originally designed for the pharmaceutical industry.

Unlike any other generic LIMS product, Qualis LIMS is a powerful enterprise-scale LIMS developed using a strong framework and is fully configurable and customizable for regulated pharmaceutical QA/QC, R&D and analytical development environment. Qualis LIMS covers all the workflow processes within a typical regulated laboratory. It addresses several pain points of the industry and saves >50% of the time and human effort with respect to data capture, review and approvals. It addresses GLP and 21 CFR Part 11/ EudraLex Annex 11 guidelines ensuring that the Organization using it in compliance to the norms.

Qualis® LIMS for Pharma - Highlights


QuaLIS® Pharma Highlights Technology

  • Multi-site and Multi lingual
  • On-premise, private or public cloud support available
  • Supports all standard browsers – Internet Explorer, Firefox, Safari & Chrome
  • Mobile Device support available – Tablets supported – iOS and Android
  • Built on a robust implementation of Java on Apache server

Technical Workflow are

  • QC ready – QC/ R&D labs
  • Configurable for Review, approval & release
  • Support Parallel & serial review
  • Support Electronic signature


  • Quality & test planning – bulk/ discrete products
  • Equipment & Instrument Management with Calibration/ Validation/ Maintenance of records
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