eConsent for Clinical Trials
Obtain informed consent from patients with Datatrak’s eConsent software to gather data directly from the patient remotely through any device. Whether your trial is hybrid or decentralized, simplify the capture of digital data from patients and sites, while enhancing the quality of data with Datatrak. Datatrak’s eConsent has many additional features than the industry standard — except for what it will cost, which is below the industry standard and far less prohibitive for study sponsors and CROs.
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Increase Patient Engagement & Retention
Harness the power of informative videos, questions to measure comprehension, diagrams, images and study retention.
Flexible Design Capabilities
Build forms the way your team sees fit and make set up a breeze with pre-built libraries of standard eCOA forms.
Ensure Accuracy
Reduce confusion and error by enforcing workflows through edit checks based on the protocol.
Natively Integrated with EDC, RTSM, eTMF, and More
Datatrak’s eConsent has many additional features than the industry standard — except for what it will cost, which is below the industry standard and far less prohibitive for study sponsors and CROs. Natively integrated with Datatrak EDC, RTSM, eTMF, and other functions for a seamless, all-in-one experience.
See How It Works
Gather data directly from patients remotely through any device
Supports hybrid and decentralized clinical trials
Simplifies digital data capture from patients and sites
Improves trial diversity by meeting DEI criteria with Datatrak DCT
Enhances data quality throughout the trial lifecycle
Integrated Solutions
View All SolutionsElectronic Data Capture (EDC)
A powerful, cost-effective EDC system that enhances data capture and cleaning with a Rapid Startup option — easy to set up and built for any study.
Clinical Trial Management (CTMS)
Manage your clinical trials from startup to close with a fully integrated CTMS giving your team real-time visibility across all studies.
Electronic Trial Master File (eTMF)
Keep every trial document compliant and inspection ready with an eTMF system that cuts costs by 62% and integrates directly with EDC.
eConsent
Simplify patient enrollment and informed consent with digital eConsent software built for decentralized and remote clinical trials.
Post Market Surveillance
Conduct post-market surveillance and Phase IV studies with acloud-based pharmacovigilance software platform built for compliance.
EMR/EHR
Link electronic medical records to your clinical trial EDC with an EHR system and EMR software built for seamless data management.
Trial Design
Work with our expert clinical trial design team to implement your study protocol and train your users to build studies independently.
Data Management
Our clinical data management team supports your data cleaning, workflows for clinical trials, and study-specific needs from startup to close.
Frequently Asked Questions
What is eConsent in clinical trials?
eConsent is the digital method for obtaining informed consent from patients participating in a clinical trial. Datatrak’s eConsent software gathers consent directly from the patient remotely through any device, and whether your trial is hybrid or decentralized, it simplifies the capture of digital data from patients and sites while enhancing the quality of data throughout the trial lifecycle.
How does eConsent improve patient engagement and retention?
Our eConsent harnesses the power of informative videos, questions to measure comprehension, diagrams, and images so patients understand what participation involves before they sign. Edit checks based on the protocol enforce workflows and reduce confusion or error, which helps keep patients engaged from the first visit through study close-out.
What makes Datatrak’s eConsent different from other platforms?
Datatrak’s eConsent has many additional features than the industry standard, except for what it will cost, which is below the industry standard and far less prohibitive for study sponsors and CROs. It is natively integrated with Datatrak EDC, RTSM, eTMF, and other functions for a seamless, all-in-one experience across the full trial lifecycle.
News & Insights
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Increase Diversity in Clinical Trials
Discussions around improving diversity in clinical trials have been ongoing for quite some time, with relatively gradual change to actual practice.
Finally Fountayn
In early 2022, we made the concrete decision to transition away from the Datatrak name and brand and rebrand to a fresh and modern look.
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Our previous post illustrated some of the most significant benefits to operational effectiveness and efficiency in clinical trials by implementing eSource practices. These advantages speak for themselves.
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All About the Acronyms
The clinical trials industry is known for it’s extensive use of acronyms, which can often be confusing for those not familiar with the field. With numerous regulatory bodies, organizations, and medical terms, it’s no wonder that the industry has a vast array of acronyms. These are used to describe everything from medical conditions to regulatory documents to save time and simplify communication.
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