21 CFR Part 11 compliant. Allows real-time data capture. Avoid duplicate data entry. Reduce on-site monitoring visits. Reduce protocol deviations. Improve site data operations.
21 CFR Part 11 compliant. Manage and share documents electronically and control who can access it. You can sign or add annotations to a lab. test or other necessary documents in just a few clicks. Organize all your documents in the same place.
Get full control of your site(s) using eClinPro-CTMS. Our platform poses integrated tools that will speed your site operations and increase efficiency – Site/Multisite Management, Calendar, Budget, Visits and Subjects Tracker, Recruitment Module, Functional Reports, and more!
Manage recruitment campaigns on eClinPro and display it on your website. Gather patient information directly into the Volunteers database: Personal Information, Dynamic inclusion/exclusion questions and Medical information.
You can chat with volunteers/subjects and have all SMS organized in one place.
Up to 10 concurrent active studies
Up to 20 concurrent active studies. This plan includes everything in "Small Business" plan + below incentives:
More than 20 concurrent active studies. Custom price will be defined based on the amount of concurrent active studies. May apply discounts up to 15%. This plan includes everything in "Medium Size" plan + below incentives:
eClinPro, LLC is an American company with a SaaS workflow for the clinical research industry providing powerful tools as CTMS/ eSource/ eDocs/ Text that facilitate the clinical trials conductions improving compliance and efficiency.READ MORE