Clinical Research IO
Clinical Research IO offers an all-in-one platform for clinical research sites, networks, academic research, and sponsors, providing a wide range of products and services to streamline and enhance clinical research processes.
Services
Clinical Research IO offers an all-in-one platform for clinical research sites, networks, academic research, and sponsors. The platform provides comprehensive support for investigator-initiated and industry-sponsored research. By leveraging its various services, sponsors can obtain faster, more reliable data while achieving significant cost savings. Additionally, Clinical Research IO supports remote collaboration and monitoring, facilitating seamless coordination and oversight of clinical research activities.
Products
Clinical Research IO offers a suite of specialized products designed to streamline clinical research activities. These include eSource for electronic source documentation, eConsent for automating informed consent processes, and Publisher for creating and managing study templates. The platform also features a Medical Record API for rapid access to electronic medical records, Reviewer EDC for reviewing and querying data in real-time, and a Site CTMS for comprehensive site management. Other products include Reporting, Patient Stipends, and eRegulatory, which digitizes regulatory workflows.
Data Security and Compliance
Clinical Research IO places a strong emphasis on data security and compliance with international regulations such as 21 CFR Part 11, Annex 11, HIPAA, and GDPR. The platform hosts its infrastructure within secure private networks via public cloud providers and has servers located in the United States, Canada, Germany, and Australia. The company also offers Single Sign-On (SSO) integration to streamline user authentication and enhance security. Tools and resources like SOP templates and validation exercises are provided to help clients achieve full compliance.
Technological Innovations
Clinical Research IO incorporates several technological innovations to enhance the efficiency and accuracy of clinical trials. Through its Medical Record API, the platform can deliver electronic medical records and clinical care insights to investigators within minutes. The centralized publishing feature, Publisher, enables the creation, versioning, and deployment of study templates. eConsent integrates with the eSource workflow to streamline the informed consent process. Additionally, Reviewer EDC allows for the real-time review and querying of eSource data by sponsors and CROs.
Study Design Marketplace
The Study Design Marketplace offered by Clinical Research IO provides pre-approved eSource study design templates. This feature facilitates efficient study setup by allowing users to access and implement well-validated templates. The marketplace aims to accelerate the initiation of clinical trials and ensure methodological consistency across studies. By providing readily available templates, the marketplace supports faster study launches and adherence to best practices in study design.