Automating Study and
Submission Documentation

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

Regulatory Compliance

Regulatory Compliance

Generate protocol and CSR documents as per ICH guidelines with the help of Machine Learning.

Faster Approvals

Faster Approvals

Reduce the number of reviews required as automation generates formatted documents, reducing errors and edits by 60 - 70%.

Reduce Authoring Time

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.

Cost Reduction

Cost Reduction

Scale down costs and improve productivity by automating study and submission document generation.

Intelligent Document Automation Enabling Faster Study Design And Regulatory Submission.

  • Compliance

    Compliance Driven

    Generate Protocol & CSR documents as per ICH guidelines

  • Dynamic

    Dynamic Templates

    Master CSR & Protocol

  • Report

    Report Customisation

    Customise study-specific protocols and CSRs

  • Intelligent

    Intelligent Mapping

    Auto and manual mapping
    using AI

  • Collaborative

    Collaborative Authoring

    Collaborate online using
    AWS workspaces

  • Submission-Ready

    Submission-Ready Document

    Generate finalised Protocol and CSR documents

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

Find out how Clinion can help you