As part of our digital strategy of improving patient and volunteers experience, CIDP has invested in a new eConsenting tool. With this new versatile approach, patients and volunteers now have the possibility of accessing the full Informed Consent and study documentation before their scheduled visit with the Investigator at the center.

The eConsent is designed with interactive features which help improve volunteer engagement and provide them with a better comprehension of study procedures.

Reach out to us to take full advantage of our new clinical trial platform