Medrio
Medrio is on a mission to ease complexity in today’s hybrid, decentralized, and site-based clinical trials by delivering a flexible suite of eClinical technologies and services, including EDC, eCOA, ePRO, eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM).
Trusted by CROs, sponsors, and sites across all therapeutic areas and trial phases from study startup and feasibility to post-market approval, we are industry-recognized for delivering eClinical software with intuitive interfaces and time-saving “drag and drop” configurations as well as high-touch customer engagement, onboarding, and support services.
Medrio’s innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.
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ePharmaSolutions
At ePharmaSolutions, we are building something new. We are not a high-tech company. We are an idea company whose thinking is highly entrenched in technology, but not limited by it. We support the drug development industry with solutions that improve the identification, activation, training and management of clinical trial sites. With new perspectives on old problems, we deliver technology-enabled solutions that help to “un-complicate” the chaos of clinical trial management. ePharmaSolutions (ePS) is a leading provider of e-clinical solutions that improve the way that clinical trial sites are selected, trained, activated, and managed. By applying fresh thinking to old problems, we deliver clever, technology-enabled solutions that empower sponsors, contract research organizations and investigator sites to “un-complicate” the chaos of clinical trial management.
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Cloudbyz eTMF
Cloudbyz eTMF solution offers a cloud-based repository of all clinical trial documents including files, images, information, etc. Digitally store, manage, and share all clinical trial-related documents with a centralized overview. Manage essential trial documents, stay inspection ready, and enable real-time visibility for CROs, sponsors, monitors, and other stakeholders in a clinical trial.
Cloudbyz eTMF is built on the cloud, enabling Sponsors, CROs, and Sites to manage their trial documents with the highest levels of efficiency and integrity. The solution benefits are listed below -
1. Secure, reliable & scalable
2. Compliant & inspection ready
3. Flexible & easy to use
4. Real-time visibility of TMF completeness
5. Collaboration with Site/ Sponsor/CRO
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CIMS Global
CIMS Global provides regulated data science platforms and eClinical solutions designed to reshape the future of clinical trials by improving the quality, efficiency, and speed of clinical trial data acquisition, processing, analysis, monitoring, and regulatory submission. Its suite includes innovative solutions such as CRE, DDM, DMC-HUB, and eBinder, along with an eClinical Suite that supports data collection, analytics, and clinical applications across every step of a trial. CRE is a multi-tenant, validated Statistical Computing Environment for compliant clinical data analysis, using R, RShiny, and the RStudio IDE within a secure, audit-ready framework that meets 21 CFR Part 11 and GxP standards. DDM is a patented Dynamic Data Monitoring platform that displays cumulative treatment effect on a trial radar screen and predicts a clinical trial’s chance of success or failure.
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