Compare IntegPro Data Integrity Audit vs. Qualis LIMS in 2025

Qualis LIMS

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Description

IntegPro is a specialized solution tailored to assist organizations in conducting risk assessments across all systems, thereby facilitating the tracking, prioritization, and management of compliance status within the company. Following the FDA's directives on data integrity, this software empowers quality leaders, departmental heads, and system owners to quickly ascertain their data integrity compliance, identify compliance deficiencies, and implement corrective measures. The application adheres to the requirements of 21 CFR Part 11, enabling seamless paperless management and monitoring of data integrity status. It is designed to be utilized by individual departments or as part of a broader corporate initiative focused on compliance with data integrity standards. With its user-friendly interface, IntegPro serves as an efficient tool for streamlining the management and tracking of data integrity processes throughout your organization. Additionally, it offers a convenient paperless solution for monitoring compliance status, ensuring that your company can maintain high standards of data integrity. The software comes ready to use, complete with pre-configured settings for immediate deployment, making it an accessible option for organizations of any size.

Description

Qualis LIMS is an enterprise-grade laboratory information management system that is widely used in various industry verticals, such as pharmaceuticals, life sciences, contract research, clinical research, and analytical and commercial sample testing. This system has integrated modules designed to manage all laboratory processes, enabling labs to perform their tasks in an automated and paperless manner while ensuring compliance with regulatory requirements and industry standards. Qualis LIMS is a digital transformation tool for laboratories, providing the following features: • Efficient management, storage, and aliquoting of samples. • Record keeping of test and experiment results, along with the management of tests, projects, samples, instruments, and inventory in a secure central database. • Compliance with data integrity and regulatory requirements such as GxP, ISO17025, 21 CFR Part 11, and EudraLex Annex 11 without compromising quality.