eProtocol Guided Walkthroughs
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.
Take eProtocol Product Tour
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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.
Timothy Warbington
CEO, Creative Medical Technology
★★★★★
“ The Support team is very cooperative and available as and when required.
Archana Bhattacharya
Sr. Manager, Public Health Foundation of India (PHFI)
★★★★★
“ Clinion's EDC is one of easiest and quickest solution for building and configuring studies.
Nikunj Patel
Director, Data Mngmt and Bio-Statistics, CBCC Global Research
★★★★★
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
