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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.
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<i class="las la-lock"></i> ROI of a LIMS Project
21 June 2018
ROI of a LIMS Project
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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.
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<i class="las la-lock"></i> How to buy the right LIMS?
18 May 2018
How to buy the right LIMS?
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<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?
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<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”
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<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?
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      8 April 2025
      Eusoft at London Lab Live 2025: between Cloud LIMS and Generative AI 
      Join Eusoft at London Lab Live 2025 to discover Eusoft IAGO, our GenAI assistant, and explore the future of labs […]
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