LIMSXL is a NABL-compliant customizable pathology lab software that supports a secure two-level authorization process. Our software is designed to manage complete diagnostic lab operations and clinical trials conducted by clinical research labs, ensuring improved efficiency, control, and compliance. Built on the same robust LIMS architecture our clinical trials management system, it enables laboratories, CROs, and research units to manage study data, volunteers, and regulatory identifiers within a single, controlled system. Key Features & Benefits: - Lab Compliance- NABL, HIPAA, CAP, ISO-15189 - Mobile App- Bookings, Reports & Patient Engagement - Software Compliance- ISO-9001, ISO 27001, SOC 2 - Fully configurable setup for Pathology Tests, Packages & Profiles. - Patient Data, Collection Centre, Corporate Health Management, Worklist, - Discount, Report Format and Revenue Sharing Management. - Barcode generation and printing with patient and test details -for accurate sample tracking. - Two-level authorization process for result approval & digital signature integration for final authorization. - Detailed transaction logs to track any changes in patient information or important data. - Easily interface with multiple laboratory devices & analysers to automate data collection and management - WhatsApp integration for direct sharing of patient reports in PDF format. Clinical Trails Parameters: - Centralized management of bioequivalence and clinical studies - BEQ Number management for bioequivalence studies, ensuring each study is uniquely identified and traceable - Study Number tracking to manage multiple trials across sponsors or protocols - Subject and Volunteer numbering to maintain confidentiality while preserving complete participant histories - Screening IDs to document eligibility assessment and retain records for screen failures - Enrollment IDs to track participants after informed consent and throughout the trial - Volunteer-Centric Document Management for Audit Readiness - Regulatory and Ethics Compliance Built into the Workflow - Structured Clinical Trial Data Across Visits and Protocols