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Use Comala Document Management workflows to reinforce your compliance policy and procedures
Automating the review and approval process to ensure that document review and approval is undertaken by the right people and changes are tracked and reported to meet requirements.
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What are the 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. |
Compliance
installComala Document Management
by getting started on the Atlassian Marketplace or through “find new apps” in your Confluence instanceapply 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! |
includes features that enable you to enforce compliance with industry standards and regulations.
For example, you can create electronic signatures and audit trails that provide evidence of document approval and compliance. You can also set up automatic archiving and retention policies that ensure documents are stored and disposed of in accordance with regulatory requirements.
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Information on how Comala Document Management can assist you with Part 11 compliance, is available in our compliance statement for FDA Title 21 CFR Part 11. |
This compliance statement was originally designed for our Confluence server and data center apps. However, many of the elements for 21 CFR Part 11 translates to Confluence Cloud with Comala Document Management solution (e-signatures).
In regard to the Atlassian Confluence Cloud environment, you will need to have a controlled environment and a working environment to help satisfy 21 CFR Part 11. To help meet this we recommend the use of our Comala Publishing app together with the Comala Document Management Cloud app.
Once pages in a space have gone through the review and approval process provided by the Comala Document Management workflow, the Comala Publishing app can be used to automatically publish and sync the approved content to another target space for your published pages. In this published space, users will have view-only rights to the published pages.
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! |
Different space publishing
Quality Management System workflow
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/wiki/spaces/CAD/pages/7794952032 in the app! |
Publishing the approved pages using Comala Publishing
Customer case studies
We have a number of our customers who use Comala Document Management and Comala Publishing as part of their review and approval document and compliance process including helping to attain FDA Title 21 CFR Part 11 in the life sciences industry.