DFconsent
Improve clinical study recruitment with a patient-centric eConsent solution
Make it easy for patients to participate in your study
Provide a superior patient experience
Participants easily consent and re-consent with multimedia engagement that keeps them informed and provides a consistent user experience across all stages of the study
Eliminate the risk and effort of paperwork
Strict version control and electronic updates make it easy to keep information updated and eliminate the risk of mishandled consent documents and data transcription errors.
Simplify and speed up the consent process
Sponsors, site managers, IRBs and ethics committees get an easy-to-use platform with configurable eIC review + approval workflows and dedicated dashboards.
Improve patient comprehension
Study participants can explore trial-specific words and concepts at their own pace and in their own language through linked text. They can also interact easily with site personnel.
Ensure FDA compliance
DFconsent dramatically improves the visibility and transparency of the consent process and ensures that digital forms are current and easily accessible at all times.
Provide a superior patient experience
Participants easily consent and re-consent with multimedia engagement that keeps them informed and provides a consistent user experience across all stages of the study
Eliminate the risk and effort of paperwork
Strict version control and electronic updates make it easy to keep information updated and eliminate the risk of mishandled consent documents and data transcription errors.
Simplify and speed up the consent process
Sponsors, site managers, IRBs and ethics committees get an easy-to-use platform with configurable eIC review + approval workflows and dedicated dashboards.
Improve patient comprehension
Study participants can explore trial-specific words and concepts at their own pace and in their own language through linked text. They can also interact easily with site personnel.
Ensure FDA compliance
DFconsent dramatically improves the visibility and transparency of the consent process and ensures that digital forms are current and easily accessible at all times.
DFconsent
No more cumbersome consent paperwork. Just an easy, open patient information exchange.
DFconsent, your eConsent solution
- Easy access for participants and site staff
- Secure up-to-date documentation
- Fewer dropouts and better study results
- Improves compliance
- Reduces transcription errors
- Globally acceptable and multilanguage
- Standalone or electronic data capture integrated solution
DFconsent meets FDA regulations for electronic informed consent (eIC)
- Our solution contains all the elements of informed consent required by HHS and/or FDA regulations 45 CFR 46.116 and 21 CFR 50.25.
- DFconsent’s eIC process is easy to understand and navigate. Users can move forward and backward within the system or stop the process at any time and continue later.
- Ensures the protection of the rights, safety, and welfare of human subjects.
Want to see DFconsent in action?
Success Story:
American Thrombosis and Hemostasis Network (ATHN) and DFconsent
Learn how DFconsent can be a success story for your clinical trial.