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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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Eusoft – More than a LIMS
Eusoft – More than a LIMS
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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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Eusoft.Lab 10 Brochure
Eusoft.Lab 10 Brochure
We think of the lab as a mix of functional completeness at the highest level and the most innovative technologies for […]
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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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