Audience

Investigators and researchers looking for a data security and management solution in order to streamline their site operations

About Clinical Research IO

The industry’s leading eSource, CTMS, and eRegulatory software for clinical trial sites. Capture source data seamlessly and in real-time with CRIO’s best-in-class electronic source. You’ll eliminate up to 90% of your paper and improve data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System. Schedule patients, track financials, streamline recruiting, and more. Introducing electronic regulatory binders fit for the 21st century, which includes the first-ever electronic delegation log — all 21 CFR Part 11 compliant. For clinical trial sponsors: conduct 100% remote monitoring of your sites’ source data and regulatory documents in a secure, online portal. Join Our Network of 500+ Clinical Research Sites From Around The World. Our mission is to help you grow your business. We do that by streamlining your site’s operations, so that your studies don’t stop just because you aren’t in clinic.

Integrations

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Company Information

Clinical Research IO
Founded: 2015
United States
www.clinicalresearch.io

Videos and Screen Captures

Clinical Research IO Screenshot 1
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Product Details

Platforms Supported
Cloud
Training
Documentation
Live Online
In Person
Support
Phone Support
24/7 Live Support
Online

Clinical Research IO Frequently Asked Questions

Q: What kinds of users and organization types does Clinical Research IO work with?
Q: What languages does Clinical Research IO support in their product?
Q: What kind of support options does Clinical Research IO offer?
Q: What type of training does Clinical Research IO provide?

Clinical Research IO Product Features

Clinical Trial Management

Patient Database
Scheduling
Study Planning
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Recruiting Management

Clinical Research IO Additional Categories