An easy-to-use, all-in-one platform for academic studies
Use CRIO on your next NIH or other Grant-funded Research Project
Configure Studies with Ease
You don't need an IT department to build your own studies. Our intuitive, library-driven study configuration lets you set up studies quickly and painlessly. You can define the visist schedule, set "anchor" dates and visit windows, assign procedures and roles, create a range of question types from single-choice through formula, build in edit checks and skip logic; employ data lists, and embed instructions directly into the data flow.
Access Through the Web and on Mobile
Our system is web-based, meaning you can access it from any device connected to the internet, regardless of operating system. Our data collection tool is optimized for a 6-10" screen size (most tablets). Use the tablet's native voice recognition feature to dictate your progress notes. Imagine ditching paper checklists, binders, and clunky EMR's. Eliminate "shadow source." Just walk into the exam room with a tablet and start collecting data!
Embed Patient Questionnaires
You can set certain procedures to be subject-only, meaning that when it's time for your patients to complete their scales, you can have them log in under their own credentials and complete their questionnaires directly. The audit trail will clearly indicate that these were completed by the subject.
Perform Quality Control
Once a visit is completed, anyone with appropriate access can view the completed source. Our system displays the data in an easy-to-read, intuitive format. If you want to query the data, simply select the data point and affix a comment. You can even use the "@" sign to direct it to a specific colleague, ensuring he or she gets an immediate email alert.
Upload, Annotate and E-Sign Documents
You can use our system to upload and archive PDFs. Or, better yet, you can use our markup tool to affix text comments, redact sensitive data, add lines, arrows, and other drawingsââ then e-sign. Our Our system will create a single queue for the Investigator to see his or her assigned documents, and a single queue for the study owner (i.e. coordinator) to see documents not yet signed by the Investigator.
Manage Your Regulatory Binders Electronically
Make your Investigator Site Files paperless. Our eRegulatory module lets you create folders and sub-folders, upload files and route for e-signature. You can set up expiration dates to recieve alerts and manage common files such as GCP certificates. Use our industry-pioneered digital delegation of authority log and associated training tracker.
CRIO's system helps researchers become much more productive, and that allows them to focus on more
- Study Template Design
- Data Collection
- QC Review
- Data Lock and Export
- PDF Routing and Mark-Up
- Electronic Regulatory
- Financial Tracking
- Patient Recruiting
- ePro System for Patient Scales
- Training Videos
- Post-Study Archiving
Security and Compliance
Our system complies with HIPAA and adheres to best practices for security, privacy, redundancy and accessibility. As long as your department can accept web-based systems, we can likely accommodate your institution's security requirements.