Stop spending months on manual protocol writing. Clinion eProtocol leverages advanced AI to automate up to 90% of your content, helping you create fully compliant clinical trial protocols in hours.
Your instant access includes guided walkthroughs for:
- The Client Admin: Learn how to create new clinical study projects, manage protocol templates, and assign Authors and Reviewers to projects with ease.
- The Author: Discover how to upload source documents, generate entire protocol sections with AI, edit content in a rich-text editor, and seamlessly submit sections for evaluation.
- The Reviewer: Experience the intuitive process for reviewing submitted content, adding contextual comments, and approving sections to ensure quality and final compliance.
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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.
“ Clinion EDC combines a strong product with reliable support, which has been essential for our studies. It is robust and easy to navigate, with features like the visit scheduler and data loader that make our workflows better and efficient.
“ I have to say that the team and database are AMAZING!!
“ The Support team is very cooperative and available as and when required.
“ Clinion’s software is simple to configure and understand.
“ The ease and speed at which a new study can be set up in Clinion is commendable. We can set up a study within two weeks.
“ Clinion's EDC is one of easiest and quickest solution for building and configuring studies.
True Trial Transformation Starts Here
Compliance
Fully Compliant with Global Standards
