EDC / ePro
Electronic Data Capture / Electronic Data Capture – Overview
Electronic Data Capture ( EDC )
Electronic Data Capture (EDC) is a cutting-edge technology that simplifies and streamlines the process of data collection in medical research and clinical trials. It is a sophisticated system designed to replace the traditional paper-based methods, making data capture faster, more accurate, and secure.
Spectral Analytics Precision Tele-Monitoring (SAPTM) EDC is designed in such a way that to capture, manage and report clinical research data – to provide immediate access and track of the data acquired from different sources.
Dynamic CRF Workflow and branching, Approvals and Authorizations within the system, configurations based on study like Clinical Endpoint Adjudication (CEA) and Query management are the key features of SAPTM’s EDC.
SAPTM EDC should be compatible with CDISC data exchanges standards and Submission Data Standards (SDS) and Study Data Tabulation Model (SDTM).
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At Spectral Analytics, we have harnessed the potential of EDC to streamline and simplify the data capture process. Gone are the days of manual data entry and paper-based forms, as our advanced EDC system empowers researchers, physicians, and patients with a modern and user-friendly interface.
With EDC, researchers can easily design electronic forms tailored to their study requirements, ensuring that data is captured accurately and consistently. Participants can access these forms securely through web applications or mobile devices, allowing them to conveniently enter their health-related information in real-time.
The benefits of EDC are manifold. By digitizing data collection, we reduce the risk of errors, eliminate the need for data transcription, and accelerate the overall study timeline. Our EDC system also boasts built-in edit checks, ensuring compliance with the study protocol and minimizing discrepancies.
Electronic Patient Reported Outcomes ( ePRo )
Electronic Patient Reported Outcomes (ePRo) is a digital web or app-based form to collect health related data about a study participant per the clinical trial protocol, which is the core part of ePRO.
With ePro, you become an integral part of the clinical trial process, enabling researchers and doctors to gain valuable insights into your well-being, treatment progress, and overall quality of life. Through simple and intuitive interfaces, you can easily answer questionnaires, record symptoms, track medications, and provide feedback on how you're feeling.
ePro supports the following data collection methods:
1. Manual entries (through web application or mobile application)
2. Automatic data transmission from smart watch and Smart phone devices
System has built in edit checks to ensure full protocol compliance with Protocol tips built into the EDC and ePro per Protocol.
Electronic Patient Reported Outcomes (ePro) is a revolutionary digital solution designed to elevate your healthcare experience to new heights. With ePro, you become an active participant in your own health, equipped with the tools to communicate with your healthcare providers seamlessly.
Imagine having the power to share vital health data with your medical team anytime, anywhere. ePro's user-friendly web or app-based form allows you to effortlessly provide health-related information that aligns with your clinical trial protocol. Whether you're tracking symptoms, recording medication usage, or answering questionnaires, ePro makes it a breeze to stay connected with your healthcare journey.
One of the exceptional features of ePro is its versatility in data collection methods. You can manually enter your information through the web application or mobile app, making it incredibly convenient for you. But that's not all – ePro also facilitates automatic data transmission from smartwatches and smartphones. This integration ensures a comprehensive and real-time view of your health, empowering healthcare professionals to provide personalized and effective care.
At the core of ePro is the dedication to your well-being. The system incorporates built-in edit checks, ensuring that your data complies fully with the clinical trial protocol. It's a seamless experience that allows you to contribute to medical research effortlessly.
To make the ePro experience even more supportive, we've integrated AI bots, CannaBot, and DrBot. These AI-powered tools serve as friendly reminders, ensuring you never miss any critical steps in your health reporting. They help you stay on track with the protocol and assist in maximizing the benefits of ePro.
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