For Sponsors and CROs

The many benefits of a new consenting standard

Q Consent™ was designed with you in mind—gain complete flexibility to offer participants a positive and engaging consenting experience while ensuring efficiency and compliance.

Know you’re compliant
and secure

Q Consent meets or exceeds stringent privacy and security requirements in alignment with industry-standard regulations, including HIPAA/HITECH, 21 CFR Part 11, and PIPEDA. And it’s the only COPPA compliant eConsent solution available.

Eliminate consent documentation errors

No need to worry about re-consenting on an old consent form or missing signature lines. With version control and error locks, your participants will only sign the most current consent form, and their consent won’t be final until all required fields are completed.

Keep metrics at your fingertips

With Q Consent dashboards, you will enjoy metrics at-a-glance. View study-wide or site-specific metrics at the click of a mouse. Plus, site monitors are able to access a site’s activity remotely.

Start your research faster

Only Q Consent combines IRB integration, earlier participant engagement, and real-time metrics to ensure your review and consent processes are the most efficient possible. Plus, our familiar interface allows your sites to forget the technology and focus on your research.

Your research sites
will thank you

Q Consent enables sites to engage with participants early and often. IRB integration, combined with real-time site enrollment metrics, results in accelerated study startup and efficient enrollment planning.

Ready to Learn More?

Request a Demo