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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.

	Document Management
Create documents from templates, manage its lifecycle through workflows. Document management is 21 CFR Part 11 compliant and supports e-signatures.

	Asset Management
Create entities, manage its lifecycle from "new" to "retirement" through workflows. Group entities into systems to create your hierarchical structures.

	Validation Lifecycle Management
Manage validation lifecycles from templates to paperless executions. Eliminate paper from validation.

	Training Management
Manage employee training and course material in compliance with GxPs. Eliminate paper, save costs and stay compliant.

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