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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.

<i class="las la-lock"></i> ROI of a LIMS Project

21 June 2018

ROI of a LIMS Project

Key Questions – How to buy a LIMS?

31 May 2018

Key Questions – How to buy a LIMS?

Download our User Requirements Checklist: a valuable tool for ensuring the LIMS will do what users need it to do.

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

18 May 2018

How to buy the right LIMS?

<i class="las la-lock"></i> What does configuration mean in terms of LIMS?

4 May 2018

What does configuration mean in terms of LIMS?

<i class="las la-lock"></i> E-book “SaaS in Cloud: The Software Model of the Future”

20 April 2018

E-book “SaaS in Cloud: The Software Model of the Future”

<i class="las la-lock"></i> Configuration tools – What does this mean in the LIMS world?

19 March 2018

Configuration tools – What does this mean in the LIMS world?