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Eusoft.Lab LIMS & FDA CFR 21 Part 11
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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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Download the white paper “Manage your lab easily”
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Download the white paper “Manage your lab easily”
Today technology offers great scope for innovation and transformation in business organizations. SaaS (Software as a Service) is currently one […]
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<i class="las la-lock"></i> Manage the lab easily – white paper
Manage the lab easily – white paper
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Eusoft presente a Paperless Academy 2015
Paperless workshop presentation
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Press Release – Eusoft Paperless Lab Academy Review 2015
Press Release – Eusoft Paperless Lab Academy Review 2015
Eusoft launched their newly developed Eusoft mobile application and hosted a workshop at Paperless Lab 2015.
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Adottare l’innovazione – leggi la nostra visione sul cloud
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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 […]
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Web based LIMS benetifs
Web based LIMS benetifs
Discover the benefits of a web based LIMS.
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