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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> How to buy the right LIMS? (Part 2)

23 January 2019

How to buy the right LIMS? (Part 2)

<i class="las la-lock"></i> How a LIMS can enhance Lab Data Quality

12 October 2018

How a LIMS can enhance Lab Data Quality

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

16 July 2018

How to buy the right LIMS?

<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?