Quality Management System & Learning Management Systemfor Highly Regulated Industries including Life Sciences, Aviation, Manufacturing

eLeaP delivers integrated software solutions for organizations in FDA-regulated industries including life sciences, aviation, and manufacturing. The platform combines Learning Management (LMS), Quality Management (QMS), and Performance Management capabilities designed specifically for environments requiring strict compliance with regulations like FDA 21 CFR Part 11, FAA 14 CFR, and ISO 13485.Learning Management System The web-based LMS uses an intuitive interface that enables both technical and non-technical users to create, track, and manage compliant training programs. Core capabilities include customizable course creation with AI assistance, observation checklists for hands-on assessments, continuing education tracking, skills and competency management, and advanced reporting that demonstrates regulatory compliance. The system supports instructor-led training, SCORM content, and self-paced learning paths.Quality Management System The integrated QMS provides document control, change management, CAPA (Corrective and Preventive Action), audit management, and supplier quality tracking. Organizations can maintain quality documentation, track non-conformances, and manage the complete quality lifecycle within the same validated environment as their training records.Performance Management System The Performance Management module enables structured performance reviews, goal tracking, competency assessments, and 360-degree feedback. Managers can link performance objectives directly to training requirements and skills development, creating a comprehensive view of employee development and regulatory compliance.Integrated Compliance Unlike standalone systems, eLeaP's integrated approach ensures consistency across training records, quality documentation, and performance evaluations. Comprehensive audit trails track user actions across all three platforms, electronic signature capabilities meet regulatory requirements, and validation documentation satisfies FDA, FAA, and ISO inspections.The cloud-based platform scales from small organizations to enterprise operations while maintaining the validation and security standards required for regulatory audits. No software installation or dedicated IT staff required, though implementation timelines vary based on organizational complexity and integration requirements.Organizations requiring validated, audit-ready systems for regulated industries can schedule a consultation to discuss specific compliance requirements.