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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 presente a Paperless Academy 2015

16 June 2015

Paperless workshop presentation

Adottare l’innovazione – leggi la nostra visione sul cloud

News

18 May 2015

White paper – Keys to success for a LIMS implementation in a laboratory – 1st part

When you hear the following sentences: “The implementation of the LIMS has been a success, everything was according to the […]

Web based LIMS benetifs

19 December 2014

Web based LIMS benetifs

Discover the benefits of a web based LIMS.