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Eusoft.Lab LIMS & FDA CFR 21 Part 11
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> LIMS implementation best practice – 2nd part
LIMS implementation best practice – 2nd part
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<i class="las la-lock"></i> LIMS implementation best practice – 1st part
LIMS implementation best practice – 1st part
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Adottare l’innovazione – leggi la nostra visione sul cloud
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Read the white papers about LIMS best practices
If you hear the following sentences: “The implementation of the LIMS has been a success, everything ran on schedule and all […]
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<i class="las la-lock"></i> 5′ guide for LIMS as Saas
5′ guide for LIMS as Saas
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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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