Consentic offers the gold standard in clinical trial consent.
PICFs are complex and translate information poorly to study participants. This has repeatedly been demonstrated in clinical studies to be a reason for non-participation.
The average time to consent a patient for a clinical trial is at least two hours.
Proprietary consent animations, that distill complex information from your study protocol into simple to understand animations.
Engaging electronic consent forms and interactive checklists, that the study participant completes prior to signing an electronic consent form.
Consent patients remotely, in the comfort of their own home, or in the clinic / clinical trial centre.
Our simple to understand animations save hours of staff recruitment time whilst improving the participants’ understanding of the consent process, allowing staff to focus on higher-value activities.
ROBUST DATA SECURITY
We have the highest standards of data protection and security, and all data is compliant.
The electronic consent process captures the process every step of the way, allowing a robust recording of the consent process and a final electronic consent form.
BETTER PATIENT EXPERIENCE
We are evidence-based, and not only save time but enable better patient understanding and satisfaction.
Our simple to understand animations demystify complex trial information into simple concepts that patients can truly engage with.