|
|
|
What is cSAVE?
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. |
| |
| cSAVE Capabilities |
|
cSAVE provides a single integrated platform to manage your organization's assets, documents, validation and training. Employees can efficiently collaborate by eliminating paper while staying in compliance with GxPs and 21 CFR Part 11. Since cSAVE is built on familiar platforms (Microsoft SharePoint and Office), cSAVE requires very minimal training. |
|
| Document Management |
| Create documents, manage its lifecycle through workflows. Document management is 21 CFR Part 11 compliant and supports e-signatures |
| |
| Validation Lifecycle Management |
| Manage validation lifecycle from templates to paperless executions. Eliminate paper from validation. |
| |
| Asset Management |
| Create assets, manage its lifecycle from "new" to "retirement" through workflows. Group assets into asset groups to create your hierarchical asset structures. |
|
|
|
|
|
|
|
|