KIVO DMS
Automate and Optimize Your GxP Compliance Processes
Automatic naming conventions, pre-configured folders and placeholders for structured content, compliant document workflows, and more.
Compliance Simplified Through Smart Automation
Accelerate GxP Compliance with Kivo’s Automation Tools
Build to the EDM Reference Model, Kivo includes simple, smartly automated features that make it easy to enforce compliance and SOPs across your organization. Use it out of the box, or customize it to match your workflows.
PROCESS AUTOMATION
Organized Efficiency for Your Document Lifecycle
Automation for the entire document lifecycle, including:
- Automatic folder structure and document placeholders
- Increment and track document versions at every step
- Fully compliant workflows for creating, editing, reviewing, and approving documents
- Real-time reporting on document status
Structured Automation for Document Management
Enforce GxP Compliance
With 21 CFR Part-11 Compliant e-Signatures with DocuSign, approval workflows, and automatic audit trails, you'll always be GxP ready.
Real-Time Reporting
Get the status of documents across the organization instantly, sorted by product, team, or individual, so you can easily stay on top of your timelines.
3rd Party Collaboration
Document placeholders ensure that everyone - both internal and third party contributors - know where to put their documents from the beginning.
Consistent File Naming
Automatic naming conventions for all file types that meet compliance best practices, so you are always audit- and inspection-ready. Not to mention making documents easy to find!
Customize As Needed
Have your own templates, naming conventions, metadata, etc? Great! Kivo can be customized to match your workflows and processes, keeping your organization aligned and running smoothly.
Training Workflows
Ready to train on your newly approved document? Assign users to training linked directly to your document - and track training completion with real-time reports.
Accelerate Your
Workflow with Kivo
See how Kivo can help your team reduce manual work and improve compliance.
FAQs
Process automation for GxP compliance involves using tools like Kivo to automate tasks such as document management, workflows, and compliance tracking, ensuring regulatory adherence with minimal manual intervention.
Kivo offers features like 21 CFR Part 11-compliant e-signatures, automated audit trails, and approval workflows to ensure your organization meets FDA regulations.
Yes, Kivo allows you to customize templates, naming conventions, metadata, and more to align perfectly with your organization’s unique processes.
Kivo provides document placeholders and structured workflows that guide third-party contributors on where and how to upload their documents, ensuring consistency and compliance.
Kivo includes real-time reporting, allowing you to track document status across products, teams, or individuals instantly, helping you meet deadlines with ease.