Clinical Research IO
About Clinical Research IO
Clinical Research IO develops eSource technology that enhances protocol compliance and eliminates transcription errors in clinical trials. This platform significantly reduces audit risk by 70% and increases patient enrollment by 39%, saving time and costs for research sites and sponsors.
<problem> Clinical trials often suffer from protocol non-compliance and transcription errors, leading to increased audit risks and hindering patient enrollment. Traditional methods of data collection and management can be time-consuming and costly for research sites and sponsors. </problem> <solution> Clinical Research IO (CRIO) offers an eSource platform designed to enhance protocol compliance and eliminate transcription errors in clinical trials. The platform streamlines clinical trial processes, improves data quality, and enhances patient safety. By digitizing source data capture, CRIO reduces audit risk and increases patient enrollment. The system's intuitive interface and integrated workflows save research sites and sponsors time and money, while ensuring data integrity and regulatory compliance. </solution> <features> - eSource solution that drives protocol compliance and eliminates transcription errors - Central eSource and Site eSource options for flexible data capture - Reviewer EDC for efficient data review and validation - Reporting tools for real-time insights into trial performance - eConsent module for simplified and compliant patient consent management - Site CTMS (Clinical Trial Management System) for comprehensive site management - eRegulatory module for streamlined regulatory document management - AI-powered search engine for quick access to information within the CRIO Help Center </features> <target_audience> CRIO serves sponsors, CROs (Contract Research Organizations), and research sites, including site networks, independent sites, and academic research institutions. </target_audience>
What does Clinical Research IO do?
Clinical Research IO develops eSource technology that enhances protocol compliance and eliminates transcription errors in clinical trials. This platform significantly reduces audit risk by 70% and increases patient enrollment by 39%, saving time and costs for research sites and sponsors.
Where is Clinical Research IO located?
Clinical Research IO is based in Boston, United States.
When was Clinical Research IO founded?
Clinical Research IO was founded in 2016.
How much funding has Clinical Research IO raised?
Clinical Research IO has raised 16770000.
- Location
- Boston, United States
- Founded
- 2016
- Funding
- 16770000
- Employees
- 96 employees
- Major Investors
- Riverside Company