Enterprise Quality Management System for Regulated Industries

eLeaP is a unique Quality Management System that integrates Enterprise Learning Management directly into its core functionality. It automates training across Documents, Design Controls, Risk Management, Change Control, Quality Events, and Supplier Management.

SOPs become training assets that trigger assignments automatically once approved and effective. Training requirements adjust as design specifications progress through phases. Risk assessments deploy targeted training for new hazards. Document and process changes prompt immediate retraining. Quality events and supplier audits trigger competency gap analysis.Pre-built compliance templates enable rapid deployment in weeks.
21 CFR Part 11 validated and trusted by 164,000+ users across pharmaceuticals, biotechnical research, contract manufacturers, medical devices, healthcare facilities, software firms, and aerospace.

Document Control That Teaches

Your SOPs are not only controlled but also teachable. One click sends effective documents to training with automatic assignments and verification.

Robust document management tools for regulated environments.

Maintain control of SOPs, work instructions, and policies with version control, revision tracking, and automated approval processes. Changes in documents automatically notify affected employees and enroll them in necessary training.

Role-based access ensures employees see only authorized content, while approval workflows maintain document integrity and create audit trails for regulatory purposes. Automate recurring document cycles and reviews with templates to save administrative time. eLeaP integrates document control, quality management, and learning into one cohesive system, transforming compliance into a competitive advantage.