About Us

iQsols Pvt. Ltd. is an evolutionary technology company with a focus on solutions for Pharma and biotech industries. iQsols core competency lies in building solutions for Pharma and laboratory activities and solutions for international quality standards and regulatory norms like GLP, FDA, and GAMP. We have developed a portfolio of competencies out of this core competency.

The company's flagship product iQLIMS is designed using cutting edge technologies to help the Pharma/ biotech companies to comply to the stringent international regulatory norms like Electronic Signatures and Electronic Records (21CFR PART 11), GAMP etc. Implementation of iQLIMS would reduce the risk of regulatory non-conformance. It is thus an Enterprise Quality Management tool for the regulated industry.


iQsols Laboratory Information Management System (LIMS), sometimes referred to as a Laboratory Information System (LIS) or Laboratory Management System (LMS), is a software-based laboratory and information management system that offers a set of key features that support a modern laboratory's operations. Those key features include — but are not limited to — workflow and data tracking support, flexible architecture, and smart data exchange interfaces, which fully "support its use in regulated environments. The features and uses of a LIMS have evolved over the years from simple sample tracking to an enterprise resource planning tool that manages multiple aspects of laboratory informatics.

iQsols lays a strong foundation for demonstrable adherence to GMP and GLP guidelines. Its innovative design helps ensure 100% compliance addressing all the pharmaceutical lab complexities. It facilitates 100% paperless lab by automation of the entire lab information workflow from start to finish. It helps manage Lab Resources, and can also be integrated with ERP, seamlessly and cost effectively, enabling quick ROI.


iQsols developed Document Management System Software which helps to control and distribute the SOP's , STP's and other regulated documents. Document management software systems not only reduce the costs of compliance, but also help you improve process and product quality. Document Management System able to retrieve the information you need-exactly when you need it-minimizes the possibility of miscommunication and mistakes which in turn minimize risks, man hours and other documentation expenses. In other words, having the right documentation available at the right time will save organization's time and money.

iQsols QMS

iQsols QMS can be used for many reasons, including the management of compliance, facilitating the investigation of adverse events and the proceeding corrective actions, managing risk, and, among many others, integrating complaint management into the quality management process. iQsols Quality Management System Software included with the following modules but not limited to -
  • Change control management
  • Incident Management
  • Deviation Management
  • Audit Management
  • Corrective and Preventive Action Management
  • Compliance & Feedback Management
Instruments and Calibration Management
  • Instruments Log
  • Instruments Categories
  • Calibration Schedules
  • Calibration Alerts and Reminders
Stock & Inventory Management
  • Chemical Management
  • Working Standards Management
  • Reference Standards Management
  • Volumetric Solutions
  • Column Management
  • Instrumental Assets
  • Stock in Hand – All Department levels
  • Stock in QC
Sample Management
  • Batch Quantities
  • Received Quantity
  • Reconciliation Records
  • Controlled Samples
  • Expired Samples


To find out more about how working with iQsols could benefit your business please send us your question using the form below. Email us at: info@iQsols.com