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Eusoft.Lab LIMS
& FDA CFR 21 Part 11

21 May 2024

Eusoft.Lab LIMS & FDA CFR 21 Part 11

Title 21 CFR Part 11 of the Code of Federal Regulations contains the regulations concerning electronic records and electronic signatures as formulated by the US Food and Drug Administration (FDA). This document gives a brief overview of technical features of Eusoft.Lab as cloud-based LIMS Software as a Service (SaaS) which fulfils the requirements of 21 CFR Part 11 and facilitate its implementation within an organization.

Eusoft.Lab LIMS & FDA CFR 21 Part 11

21 May 2024

Eusoft.Lab LIMS & FDA CFR 21 Part 11

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