Clinical Studio is a comprehensive, cloud-based Electronic Data Capture (EDC) software that supports data managers, researchers, and clinical professionals in the collection and analysis of clinical trial data. Clinical Studio allows data entry, access, and analysis anywhere, anytime, saving time. We’re the customer data experts, with over 45 years of experience connecting customers and brands Gather Data Capture App is not just a mobile form builder. We provide all our clients with consultancy to make sure you collect only high-quality data you can use. Data Capture Technologies There are several ways of capturing and processing data electronically. Powerpro quipp 300 replacement parts. One of the most common approaches: scanning documents in to a processing system (via a standard document scanner), at which point optical character recognition ( OCR ) software is used to detect the characters on those documents and validate it against other known information (perhaps in the ERP). Data input can be performed in several ways, including by data entry. In data entry, data is placed in chosen fields of a database by a human agent using a device such as a mouse, keypad, keyboard, touch screen, or stylus, or alternatively, with speech recognition software. Data capture is a kind of data input in which there is no data entry.
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Castor EDC is a cloud-based Electronic Data Capture, eCRF, ePRO, eCOA and eTMF platform that enables researchers to easily capture and integrate data from any source in real-time. Highlights: Build a study within hours; Capture EMR, patient, clinician, and device data (ePRO, eCOA, eCRF) on a central platform; Maximize value of study data and reduce time-to-market; Monitor study progress using real-time reporting; Compliant with 21 CFR Part 11, GCP, GDPR & HIPAA; ISO27001 & ISO9001 certified Learn more about Castor EDC
![]() Data Capture SystemsCastor EDC is a cloud-based Electronic Data Capture, eCRF, ePRO, eCOA and eTMF platform that enables researchers to easily capture and integrate data from any source in real-time. Highlights: Build a study within hours; Capture EMR, patient, clinician, and device data (ePRO, eCOA, eCRF) on a central platform; Maximize value of study data and reduce time-to-market; Monitor study progress using real-time reporting; Compliant with 21 CFR Part 11, GCP, GDPR & HIPAA; ISO27001 & ISO9001 certified Comments are closed.
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