Built for Sites, Better for Your Trials. Clearly CRIO

Screenshot of the CRIO platform showing the ‘Informed Consent’ section for a subject named Abigail Jones during Visit 1 - Screening. The screen is titled ‘Test Study’ and the user logged in is Raymond Nomizu. A pop-up window titled ‘Launch Signature’ is open, offering ‘In Person’ and ‘Remote’ signing options. The pop-up includes fields for sending a PIN via phone (111-555-7283) or email (partially filled as ‘abigail’). Navigation menu items on the left include Informed Consent, Demographics, Alcohol Use Status, Concomitant Medications, Complete Physical Exam, 12-lead ECG, Standard Vitals, Inclusion Criteria, and Complete Visit.

Intuitive eSource Enabling Faster, Smarter Decisions

You need reliable, protocol-driven data, but sites can’t focus on quality when bogged down with administrative details and manual tasks. There’s an eSource solution that makes it all easier.
It’s clearly CRIO.

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Your eSource Solution

CRIO is an intuitive eSource solution that collects data directly at the point of patient interaction to lighten site burden while driving protocol compliance. Created by a team of clinical research experts who understand what sites need to perform better, it’s built to make trials run seamlessly from the start:

  • Fully configurable and scalable templates standardize data capture

  • Real-time data access enables remote monitoring and collaboration

  • Easily accessible reporting and query capabilities enhance data quality and site performance

  • A connected ecosystem supporting essential data collection activities streamlines workflows

See CRIO in Action

  • 40% Higher Enrollment

  • 40% Faster Startup

  • 40% Fewer Protocol Deviations

I think of Central eSource as the next evolution in clinical trial efficiency, similar to the shift toward central IRBs and central labs. It ensures high-quality data by standardizing critical data points, yet empowers sites to configure the system to align with their own local practices. Central eSource speeds up study startup considerably. Everyone benefits.

Takoda Roland, Associate Vice President of Customer Success, Sitero

As a tech-enabled, virtual CRO, we have incorporated CRIO as a core technology to deliver streamlined and compliant data for our sponsor clients. Our digital-first design philosophy, combined with CRIO’s site-centric approach, deliver unique value and faster timelines across virtual, hybrid and traditional study structures.

Lorraine O’Donnell, Director, SN Research

CRIO’s Reviewer interface is intuitive and easy to use, and with direct data capture, sponsors have a cost effective tool to take more clinical trial oversight in house.

David Goffredo, Associate Director Clinical Projects, RxSight, Inc.

In research, one error can cause a lot of bad consequences like an audit, loss of business, etc. With CRIO, I know I have a much lower chance of something like that happening. I can go to sleep at night knowing we have quality under control. This is my livelihood, so there is no price tag to that peace of mind.

Dr. James Clark, Principal Investigator (now with Alcanza)

I highly recommend sites, sponsors and CROs implement CRIO across their trials. It’s a powerful, purpose-built clinical research tool that ensures protocol compliance upfront.

Dr. Elena Christofides, CEO, Endocrinology Associates

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