Reducing Audit Findings with a Validated LMS

Is Your Organization Audit-Ready?

Regulatory scrutiny is more intense than ever, and non-compliance can result in costly penalties, delayed approvals, and reputational damage. A validated Learning Management System (LMS) is critical for managing training, maintaining compliance, and reducing audit risks in life sciences, pharmaceuticals, and other regulated industries.

This in-depth 12-page white-paper shares insights from our 21 CFR Part 11 experts on topics including:

• How a validated LMS simplifies training compliance and record-keeping
• Ways to automate audit trails and minimize human errors
• Key regulatory requirements, including 21 CFR Part 11, EU Annex 11, and ISO standards
• The role of training documentation in audit preparedness
• How eLeaP helps organizations maintain compliance, efficiency, and security

Ensuring compliance and reducing audit risks requires the right tools and expertise. eLeaP’s validated LMS is designed to help regulated organizations meet stringent FDA, EMA, and ISO requirements with confidence. Whether you need assistance with LMS validation, compliance tracking, or audit preparedness, our team is here to help.