Document Automation

CLINION Document Automation

Automating Study and
Submission Documentation

Leveraging AI to automatically generate CSR documents, Clinion CSR automation helps you reduce submission timelines for all clinical trial documents by weeks

About Document Automation

Automate Protocol And Clinical Study Reports with AI

See Clinion in action

Faster Study Design And Regulatory Submission

Intelligent Document Automation

Automate Protocol And Clinical Study Reports With The Help Of Machine Learning

Reduce Authoring Time

With the auto-generation of 60-70% of study and submission documents within minutes, medical writers experience tremendous time savings from authoring reports manually.

Submission-Ready Document

Generate finalised Protocol and CSR documents

Intelligent Document Automation Enabling Faster Study Design And Regulatory Submission

Regulatory Compliance

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Faster Approvals

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Reduce Authoring Time

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Cost Reduction

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Speed up your entire clinical trial process from protocol creation to CSR submission

Ensure compliance

Ensure compliance by generating Protocol & CSR documents following ICH guidelines.

Utilize dynamic templates for master CSR & Protocol documents.

Customize study-specific protocols and CSRs with report customization.

Intelligent AI mapping

Employ auto and manual mapping using intelligent AI mapping.

Collaborate online with collaborative authoring using AWS workspaces.

Generate submission-ready Protocol and CSR documents efficiently.