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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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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CSAM Registries
CSAM’s Registries platform (previously MedSciNet Registries) provides a rich and versatile online environment for hosting registries, featuring powerful tools for all phases of the project’s life cycle, from data collection to analysis. CSAM’s Registries system design draws on our decade long experience of developing web-based software for medical research and offers a sophisticated online application package for hosting, maintaining, and monitoring registry projects of every size and scope. CSAM’s standard registry system implementation features a complete set of components required for setting up a fully functional registry. The system provides support for sophisticated data entry forms, flexible workflow structures, and advanced data validation, monitoring, and analysis.
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BizNet
Built for the evolving needs of pharmaceutical, biotech, and CRO organisations, our AI-enabled Clinical Research Platform unifies Early Phase CTMS, Late Phase CTMS, and Bioanalytical LIMS into a single, GxP-compliant ecosystem. It streamlines the entire clinical development lifecycle, from volunteer and patient management, study execution, sample tracking, and bioanalytical workflows to data review, reporting, and regulatory compliance. Powered by AI-driven automation, predictive insights, intelligent workflow orchestration, and real-time analytics, the platform enhances data integrity, accelerates decision-making, minimizes manual effort, and improves operational efficiency. With seamless system integration, audit-ready processes, and support for global regulatory standards such as 21 CFR Part 11, GLP, GCP, and GxP, it enables faster, scalable, and compliance-driven clinical trials with superior quality and patient-centric outcomes.
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