Product Overview
Improve clinical study recruitment with a patient-centric eConsent solution
DFconsent engages participants with interactive multimedia in their local language so they can make informed decisions about their participation in your research – and give quick consent right from their phones.
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.
Deployment
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
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.
About the company
Founded in Seattle, DFnet seeks to provide accessible and efficient data analysis, data management, and data science resources focused on public health. With the combined skills of clinical researchers, data managers, and software developers, we embark on an important mission: supporting and improving pivotal research on a global scale.
Though we may have officially introduced ourselves as DFnet in 2004, our roots go much deeper. In fact, we’ve been around longer than electronic data capture itself — the “DF” in our name stands for “DataFax,” an homage to the fax machines we initially used for research. By bridging paper case report form and electronic data capture, we developed a strong background and a thorough understanding of the methods used to record global research. For over 30 years, we have brought experience and precision to clinical trials and studies.
