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    Please Note:
    Due to the COVID-19 (coronavirus) the Innovation Forum
    has been postponed until further notice.

Expanding the Borders of EDC

Showcase. Network. Engage.

Innovation Forum is made possible in part to the support of our dedicated partners.  


Bio-Optronics is a leading software and services company that creates user-focused applications for healthcare organizations that positively impact business performance. With applications focused on clinical research, automated resource utilization and patient safety, we will be showcasing the TrialOne integrated Momentum Phase 1 Scheduling. Momentum is a leading physician and staff scheduling system in use by practices and large hospital systems in over seven countries, with extensive functionality, automation, and configurability that phase 1 researchers require in a centralized scheduling solution. The fully integrated Momentum intelligent scheduling includes automated on-demand scheduling using real-time TrialOne data, intelligent association with specific studies, flexible shift length variability, mobile access and actionable reports.

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ClinConsent is an electronic informed consent application for CROs, Research Institutions and Hospitals of any size that are looking to improve patient consent time and cut down on paperwork. ClinConsent ensures a seamless patient journey and consistent user experience across all stages of the study with consent and re-consent process, and the only electronic informed onsent solution that can serve as a standalone solution, or fully integrate with EDC or EHR platform.

ClinConsent removes the risk of mishandled consent documents and subsequent issues in regulatory inspections. It simplifies the Informed Consent for Sponsors, Site Managers, IRB, and Ethics Committees with an easy-to-use technology platform and configurable workflows. This dramatically improves the visibility and transparency of the Consent process and leads to improved compliance.

A versatile product that can be used on most devices and across different platforms. Simple, user-friendly Electronic Consent. Patient-centric design keeps engagement and adherence up, while site staff are freed from time-consuming explanations and able to focus on higher value patient focused efforts.

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Radiant Sage provides clinical image management solutions for the pharmaceutical, device, bio tech and research organizations involved in drug discovery and research.

We have developed our solutions based on a deep understanding of the imaging clinical trial process, FDA's regulatory requirements and the unfulfilled needs of the trial sponsor and various participants in the trials.

The solutions (Core-Lab-in-a-Box™ and RadVista Viewer) are designed to enable a sponsor to quickly set up a trial with custom or predesigned standard workflows as required by the protocol and begin collecting the required data within a few weeks. And all this can be done without having to invest in additional capital infrastructure using our SaaS delivery model. In addition, the sponsor has the option to manage the entire trial in-house using its own resources thus saving money and avoiding delays due to the long lead times required for identifying and, implementing the traditional out-sourcing options.

So, whether you are looking for a solution to run a small proof-of-concept trial or need to take control over the imaging data of a large phase 3 trial and integrate it into rest of the trial, Radiant Sage has the solution.



Email for a Partner Package Today.

To find out how you can be an Innovation Forum 2020 Partner, please send an email to marketing@omnicomm.com.


Contact Us      North America +1 877.468.6332      Europe +49 (0) 228 227 440      Click Here to Email Us

Contact Us
North America
+1 877.468.6332
+49 (0) 228 227 440
Click Here to Email Us