eConsent
Electronic informed consent and patient enrollment system for Face-to-Face & Remote process
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Face-to-Face/Remote electronic informed consent form that allows explanation and consent online without visiting a site
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Version controlm, e-sign audit trail, consent log and progress check
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Automatic registration to EDC&DDC
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Used at over 80 clinical trial sites
Improved patient experience, Faster and more secure than paper
Dedicated eConsent development team and rich experience in study implementation for local and overseas studies.
Related DCT Process
cubeCONSENT 3.0
Solution
Causes of recruitment failusre check
& Risk mitigation plan
More >
Recruitment plan development
Recruitment strategy
MediCLEO
More >
Patient-Reported Outcome
EDC(DDC) auto-registration
cubeCDMS 1.1 / cubeDDC 1.0
Clinical data capture
e-Recruitment
cubePRO
Telemedicine
(TBD)
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Patient app for remote full procedure
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Multimedia technology to improve the accessibility of applicants (e.g. the disabled)
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Digitally processed safe and independent system
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Possible to consider and agree on the participation regardless of place and time
For clinical trial applicant
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Time and cost saving against paper-based process, electronic distribution and collection
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Audit trails by sections in eConsent form, making it easy to manage and track consent dates and versions of each consent document
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Web administrator interface, real-time consent status check and batch download of signed copies
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System validation check to prevent data errors and omissions from subject, and verify entire information before submission
For site
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Patient app for remote full procedure
-
Multimedia technology to improve the accessibility of applicants (e.g. the disabled)
-
Digitally processed safe and independent system
-
Possible to consider and agree on the participation regardless of place and time
For clinical trial applicant
-
Time and cost saving against paper-based process, electronic distribution and collection
-
Audit trails by sections in eConsent form, making it easy to manage and track consent dates and versions of each consent document
-
Web administrator interface, real-time consent status check and batch download of signed copies
-
System validation check to prevent data errors and omissions from subject, and verify entire information before submission
For site
Proven functions and operability
Simple e-sign process for applicants and investigators
Signature pad and e-sign available for Face-to-face / Remote environment
E-sign for applicant, legal representative, witness, and CRC
Multimedia insertion for better comprehension
Enhanced understanding on the study with voice, video, and image, etc.
Simple e-sign process for applicants and investigators
Signature pad and e-sign available for Face-to-face / Remote environment
E-sign for applicant, legal representative, witness, and CRC
Multimedia insertion for better comprehension
Enhanced understanding on the study with voice, video, and image, etc.
Form development and version control
eICF Built-in editor
PDF upload by section
eICF management and version control
Signed PDF consent document upload
Remote monitoring
Consent progress and retention status check
Form development and version control
eICF Built-in editor
PDF upload by section
eICF management and version control
Signed PDF consent document upload
Remote monitoring
Consent progress and retention status check
Signed copy delivery via email/SMS
Automatic delivery to the investigator and the applicant by email or SMS
Experience with over 80 clinical sites in local and overseas
10+ major clinical trial sites in Korea (as of Oct. 2023)
Signed copy delivery via email/SMS
Automatic delivery to the investigator and the applicant by email or SMS
Experience with over 80 clinical sites in local and overseas