Features & Benefits | Example | |||
SYSTEM |
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Portability | 7" Tablet only weighs 13 ounces, and fits easily into purses & small bags | ||
Instant Data Sharing | Always connected (using Cellular Network) to allow study team instant access to critical data | |||
Multiple Language Support | Can support multiple languages, as needed, based on study requirements (including Hebrew, Japanese, Indian and more) | |||
Highly Customizable | Any event or episode can be recorded on the eDiary, based on study requirements | |||
Email & SMS Text Alerts | Alerts can be issued to study team based on patient compliance or safety concern. Alerts & reminders can also be issued to patient to improve compliance and engagement. | |||
IMPROVED DATA QUALITY |
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Accuracy | Checks data upon entry for format, range, type and allowable values | ||
Completeness | Ensures data fields are complete | |||
Consistency | Data collection is consistent across all users and countries | |||
Quality Assurance | Daily Events screen makes it easy for patient to review and update data before submission. | |||
COST SAVINGS |
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Monitoring Costs Decrease | Eliminate Source Data Verification | ||
No Data Entry from Paper | Eliminate Transcription Costs & Errors | |||
Significantly Reduce Queries | Lower Costs and Data Management Time | |||
Labor Costs Reduced | No Printing, Proofing, Distribution, etc. | |||
IMPROVE COMPLIANCE |
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Real-Time Quality Checks | Question responses & Events entries are checked for completeness and compliance, before being saved. | ||
Real-Time Compliance Monitoring | Daily Reports can be reviewed by SC to monitor compliance. | |||
Message Alerts & Media Updates (Patient) | Messaging and media are used to engage the patient and improve compliance (including email, text, games, trivia, study status, and newsletters). | |||
IMPROVE MEDICAL SAFETY |
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Medical Standards Enforced | (option) Undesirable events can be reported in real-time, and handled with appropriate intervention. | ||
Alerts | Custom email or text messages alert staff immediately of potential safety events. | |||
Efficient Adverse Event Processing | PI can be alerted (via email or text) regarding any potential AE | |||
Consistent Training | Customized training modules enforce system understanding, before being granted access. |
According to the FDA guidance on source data in electronic form, eSource will help to eliminate unnecessary duplication of data, reduce the opportunity for transcription errors, promote the real-time entry of electronic source data during subject visits, ensure the accuracy and completeness of data, and more.
assisTek's TotalSource solutions capture these improvements to source data, and are customized to each individual protocol. | More Information |
assisTek successfully fuses new developments in mobile technology with creative software solutions to revolutionize the collection of data from patients and clinicians in clinical trials. We have proudly been helping clinical trial teams achieve success for over 18 years, in 40 countries with 46 languages. Our expertise can support studies in any phase.
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