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Mednet eConsent

iMednet’s Electronic Informed Consent (eConsent) was developed within the iMednet platform to seamlessly integrate, ensuring a secure, simple and efficient electronic consent process for both study participants and site users Read More...
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Realtime eReg

Realtime eReg simplifies and streamlines compliance for clinical research sites. It replaces traditional paper-based binders with a powerful, secure electronic regulatory management system. Realtime eReg provides a centralized platform that Read More...
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Telemedicine ePRO/eCOA

Available on the Web and on any mobile support (tablet and Android or IOS smartphones), our ePRO/eCOA (electronic Patient Reported Outcomes/electronic Clinical Outcome Assessments) solution allows seamless data capture by Read More...
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Mono Software eCTD

Mono eCTD Office is a suite of integrated software products for the creation, validation, publishing, viewing and manipulation of regulatory documentation for electronic submissions by pharmaceutical companies to regulatory authorities. Read More...
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Cluepoints RBQM

Cluepoints RBQM

Leverage cutting-edge advancements in statistics and Machine Learning (ML) with AI-powered clinical trial solutions that go beyond traditional data analysis. By adhering to FDA and ICH guidelines and regulations, we Read More...
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R Project

R is a language and environment for statistical computing and graphics. It is a GNU project and provides a wide variety of statistical (linear and nonlinear modelling, classical statistical tests, time-series Read More...
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Chronicles CTMS

Chronicles RT proceeds with a project with central data review. Chronicles CTMS allows investigators to upload pseudonymized MRI and CT source data into the system for further analysis by a Read More...
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betterclinical showcases over 400 clinical trial software

For an infographic representation of all these software solutions, have a look at the Clinical Trial Software Landscape.

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