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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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<i class="las la-lock"></i> How to buy the right LIMS (Part 2)

23 January 2019

How to buy the right LIMS (Part 2)

Today LIMS are in the fourth generation of evolution and many organizations are faced with the need to upgrade, supplement […]

<i class="las la-lock"></i> How to buy the right LIMS

16 July 2018

How to buy the right LIMS

Eusoft – More than a LIMS

21 May 2017

Eusoft – More than a LIMS

Overview Eusoft Lab

21 May 2017

Overview Eusoft Lab