TrialKit
TrialKit is a unified eClinical platform designed to support the full lifecycle of clinical trials, from study design through data analysis. Built for sponsors, CROs, and research sites, TrialKit combines EDC, ePRO/eCOA, eConsent, RTSM, medical coding, imaging, and more in a single configurable system.
Its drag-and-drop study builder enables rapid setup of compliant studies without programming, while web and native mobile apps support secure, real-time data capture from any location. TrialKit AI extends the platform with advanced analytics, study simulation, and protocol validation, helping teams evaluate design decisions and identify risks earlier.
With API-based integrations and support for global compliance standards, TrialKit reduces system fragmentation, improves efficiency, and provides a scalable foundation for modern clinical research.
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Omda MedSciNet
Omda MedSciNet solutions improve the quality, utility, and management of medical data from collection to analysis. This secure standardized software makes it easy for clinical researchers and other professionals in medicine and academia to gather and analyze well-managed medical data. The Omda team specializes in building and managing tailor-made database applications and designing clinical studies for medical research and quality registers. The Omda MedSciNet study platform provides a reliable, feature-rich, and highly customizable online environment for hosting and managing sophisticated study and clinical trial systems. Omda MedSciNet has a 20-year track record of successfully hosting studies and clinical trials of all scopes and sizes. The standard implementation includes a comprehensive set of components necessary for establishing fully functional studies or clinical trials.
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BizNet
Sarjen delivers an AI-enabled Clinical Trial Management System and Bioanalytical LIMS that drives digital transformation across early-phase and late-phase clinical trials. This integrated eClinical platform supports end-to-end trial management, site management, subject tracking, regulatory compliance, and real-time laboratory sample management within a unified ecosystem. Built for pharma, biotech, and CRO organisations, the software enhances operational efficiency through workflow automation, centralised data management, and advanced analytics. Its AI features include predictive enrollment forecasting, risk-based monitoring insights, anomaly detection in lab data, automated query resolution, and intelligent dashboards that improve decision-making. By leveraging machine learning and smart automation, the platform accelerates study timelines, improves data quality, ensures compliance readiness, and transforms clinical research operations!
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Mosio
Mosio enables research teams to improve subject adherence, communications, and data collection on mobile’s most popular channel: text messaging.
Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones.
WHO WE HELP:
+ Clinical Trial Sponsors (Pharma and Biotech)
+ Cancer Centers and Clinical Research Organizations
+ NIH-Funded Studies
+ Public Health Agencies
+ Clinical Trial Managers, Clinical Operations Managers/Directors, Clinical Project Managers, Principal Investigators, Clinical Research (Study) Coordinators, and any research staff who communicate regularly with study participants.
BENEFITS:
+ Interactive dosing reminders and medication adherence alerts.
+ Automate data collection.
+ Increase engagement and adherence.
+ Fix your no-show problem with SMS appointment reminders.
+ Improve retention with automated check-ins.
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