Electronic Informed Consent for Clinical Trials

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Features

SecureConsent makes the consenting process more efficient and effective
for staff, patients, sponsors, and monitors.

  • Multimedia education for patients

    Video and audio interventions Improve patient understanding and retention

  • 21 CFR Part 11 and Annex 11

    SecureConsent is a validated part of your regulatory-compliant system.

  • Realtime monitoring and tracking

    Get unprecedented detail about how patients read and understand consent documents

  • End-to-end document management

    Eliminate common errors in paper consent like wrong versions and bad signatures

Works on Any Device

SecureConsent runs on tablets, phones, desktops, and more.
We can provide the devices or you can use your own (B.Y.O.D.).

Designed for Patients

With SecureConsent, documents are easy to read for all patient populations. Elegantly designed to focus attention,
our system offers multimedia interventions in the form of explanatory videos, audio narration, and glossary terms.

Advantages

SecureConsent has been pioneering electronic informed consent (e-Consent) since 2003. Since then, we’ve worked with patients, IRBs, CROs, sponsors, and the FDA to deliver the best informed consent process possible.

  • Better-informed patients
  • Always up to date
  • No paperwork
  • Remote monitoring
  • Fully validated

Many Applications

  • Video Consent

  • Clinical Trials

  • Procedural Consent

  • Remote/Virtual Consent

  • Biobanks/Medical Registries

See a demo today

SecureConsent is available for studies and institutes of all sizes.

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