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Excerpt

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hiddentrue

Learn more about CommCare’s usage by universities and research teams.

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Our Mission & Impact

Dimagi envisions a world where all people have access to the services they need to thrive. We contribute towards that vision by building sustainable, high-impact digital solutions that amplify frontline work.  CommCare is our most widely used frontline solution –– and the most widely-deployed technology platform for frontline work. With 80+ peer-reviewed studies, CommCare has the widest evidence-base of any mobile platform for frontline work. 

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Research is indispensable for resolving global development challenges – whether it be tackling diseases of poverty, responding to the rise of chronic diseases, or ensuring that mothers have access to safe delivery practices.  CommCare is proven to be effective across the entire lifecycle of frontline research, right from observational studies, experimental research, intervention research through to programmatic implementations at scale.  While CommCare is commonly used for public health studies, it is used across disciplines, such as agriculture, education and sanitation. 

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ACIAR, AMREF, BRAC, Boston University, Duke University, Emory University, Georgetown University, Harvard University, ICAP at Columbia University, icddr,b, KEMRI,London School of Hygiene & Tropical Medicine, Mbarara University of Science & Technology (MUST), UCSD, UCSF and UNC. 

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CommCare is HIPAA compliant. However, we sign HIPAA BAAs with partners using the CommCare Advanced software plan or above. 

CommCare is 21 CFR Part 11-ready, meaning that if implemented in conjunction with appropriate procedures, documentation, and qualification, then your study may meet part 11 requirements. CommCare has the technical features necessary to serve as the data collection and management component of a 21 CFR Part 11 compliant study. However, a study using CommCare must have policies, procedures, training, validation and documentation meeting the requirements of Part 11 and the predicate rules for the underlying legislation. An FDA auditor will review all project documentation to determine at the study level if a study is compliant.

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