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Use Comala Document Management workflows to ensure that policies and procedures are up-to-date, consistent, and secure
Automating the review and approval process to manage the lifecycle of your policies and procedures can ensure that critical documents do not become stale and out-of-date.
What are ways teams benefit?
Compliance
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Minimize the risk of errors by ensuring that documents are reviewed and approved by the correct people. Track and report all changes and approvals, mandatory for meeting regulatory standards. This protects your company from legal liability while strengthening its reputation |
Knowledge Bases
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Provide clear visibility into the documentation lifecycle status so knowledge workers see
This increases the accuracy of documentation and reduces the risk of misinformation. |
Policies and procedures
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Reduce the chance of accidents, compliance violations, and other problems by automating workflows to manage the lifecycle of your policies and procedures. Set expiration dates so that you’re notified when it is time to review and update your processes. This ensures that policies and procedures are up-to-date, consistent, and secure. |
To get started
install Comala Document Management by getting started on the Atlassian Marketplace or through “find new apps” in your Confluence instance
apply a workflow at across all documents in a space or apply workflows on a page-by-page basis
configure your workflow in the space settings Comala Document Management dashboard
edit and customize your workflow using the workflow builder visual workflow editor for advanced authoring to create a more flexible and responsive workflow for your document process needs
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Choose from the “out of the box” workflows or create your own! |
Content expiry workflow
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“Out of the box” workflow in the app! |
Customer case studies
We have a number of our customers who use Comala Document Management as part of their review and approval document management process. These include some customers who use our app together with Comala Publishing to help attain FDA Title 21 CFR Part 11 in the life sciences industry.