Never miss another re-consent with CRIO eConsent, an integrated eConsent-eSource solution

There is a common problem with most eConsent solutions: they don’t solve the “re-consent problem.” In the majority of clinical trials, sponsors make mid-study amendments to the protocol, which necessitate a new version of the Informed Consent Form (ICF). ICH-GCP principles require that the investigator execute the new version of the ICF with an enrolled patient prior to performing any procedures under the new amendment – this re-consent is usually done at the outset of the patient’s next visit.

CRIO’s integrated eConsent-eSource solution addresses this issue. Download this white paper to learn more about the differences and the benefits of an integrated eConsent-eSource solution.

Learn More About CRIO

SCHEDULE A DEMO TO LEARN ABOUT OUR PRODUCTS

Give us a call:
617-302-9845

Email:
Sales@clinicalresearch.io