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cSAVE is a an integrated software suite that has been designed to help
improve business process efficiencies in FDA regulated industries. cSAVE
is a configurable product that provides document management, validation
lifecycle management, asset management and training management
modules. cSAVE enables GxP companies to implement best practices while
eliminating paper completely. You can save significantly while increasing
your compliance score.
You can manage entities and their validation lifecycles, collaborate on
validation projects and manage your employee training programs. You
can even automate traceability and risk assessments.
cSAVE is built on information platforms you already own - Microsoft
SharePoint and Microsoft Office. |
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Details |
| Explore
product details and learn how various modules can be configured to comply
with industry standards such as GAMP5 and ASTM-E2500. | |
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Capabilities |
| Learn how cSAVE's capabilties and
features can benefit your organization. Explore how it can help your
organization eliminate paper and streamline your business processes. | |
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Editions |
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Select the best edition that meets your organization's
needs. | |
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