CSR Automation Guided Walkthroughs
This guided walkthrough demonstrates our end-to-end, role-based workflow. You will see firsthand how Clinion CSR Automation streamlines setup, automates content generation, and accelerates review cycles to produce submission-ready reports with unparalleled speed and accuracy.
This guided tour includes:
- Admin Setup: See how a Client Admin creates projects, manages user accounts for Authors and Reviewers, and sets up ICH E3-compliant report templates.
- AI-Powered Authoring: Watch as an Author uses the system’s Generative AI to automatically extract content from uploaded source documents like the Protocol and SAP to generate a well-structured draft.
- Collaborative Review: Discover the seamless review cycle where a Reviewer can add inline comments, view revision history, and approve sections, moving the report efficiently toward finalization.
Take CSR Automation Product Tour
Awards & Recognitions
Achievements in Clinical Excellence
Clients Testimonials
What Our Customers Say About Our Services
“ We didn’t think setting up a study in two weeks was possible until we used Clinion’s EDC. It’s intuitive, well-designed, and feels like it was built just for us. If you're looking for an innovative, robust EDC that truly supports you, this is it.
“ The Support team is very cooperative and available as and when required.
“ Clinion's EDC is one of easiest and quickest solution for building and configuring studies.
Unlock the Future of Clinical Trials with Clinion.
Cut your trial costs by 35% and accelerate your time-to-market by 30%
Compliance
Fully Compliant with Global Standards
