Learning management system (LMS) reporting: Formatting for regulatory audits
A life sciences company’s learning management system (LMS) should feature reporting tools that capture employee training records, including validated and unimpeachable electronic signatures.
Companies require LMS technologies to provide reports that should be easily accessible, in un-editable and easy-to-read formats that can be provided to US Food and Drug Administration (FDA) inspectors and other regulatory auditors when requested. The Electronic signatures in LMS reports must meet FDA 21 CFR Part 11, EU’s Annex 11 and other global regulatory bodies’ requirements.
Companies require LMS technologies to provide reports that should be easily accessible, in un-editable and easy-to-read formats that can be provided to US Food and Drug Administration (FDA) inspectors and other regulatory auditors when requested. The Electronic signatures in LMS reports must meet FDA 21 CFR Part 11, EU’s Annex 11 and other global regulatory bodies’ requirements.
