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Dacima’s eConsent improves trial participants experience by meeting them where they are.
It enables the improved quality and efficiency of clinical trials through insight into the patient experience, improves data quality and a fully electronic experience. 

Dacima’s EDC/eSource includes a fully compliant eConsent solution that allows for both in person digital consenting and remote consenting of patients.  The software allows to simplify the consent process, raises patient comprehension and retention, and eases workloads for study teams and sites. The flexible and powerful design features allow a sophisticated and intuitive electronic informed consent (eICF) with videos, graphics, and PDF files.


  • Integrated electronic informed consent with existing EDC/ eSource Dacima Clinical Suite platform eliminating separate systems and reconciliation.
  • In person eICF, through sharing  your tablet with the patient or pushing the eICF to kiosks/tablets in waiting rooms.
  • Remote consenting allows user to send eICF link email or SMS.
  • Self-recruitment allows patients complete eICF after registering and creating an account for the study through a lobby page.
  • Real-time subject status tracking for seamless patient recruitment and data collection.
  • Wide range of eConsent design capabilities including  embedded  video, graphics, PDF files for patients to review,  consent acknowledgement checks.
  • Ability to create multistep inclusion process for screening, consenting, eligibility checks and/or randomization.
  • Ability to create multiple consents within the same study.
  • Dynamic visit creation, form activations and conditional logic to configure different workflows.
  • Required signatures (CFR Part 11 compliant for patients signature and option for clinicians/investigators signatures).
  • Electronic informed consent form (eICF) signing triggers