So how does it work?
1. Researchers can create studies, add multiple languages, data entry forms, create logic, and funnel participants to generate RWD for research, collect patient-reported outcomes, conduct population studies.
2. Researchers can then onboard the participants, track and manage consent documents and participation status of the patients through the administrative panel.
3. Patients/participants can connect to the researchers or organization page by using a unique link, and see the available studies. Patients can read study details, consent documents and proceed to view available data entry forms in the study.