patients & caregivers are in full control of the data they contribute towards clinical research
patients & caregivers receive customized insights, data and other digital services to help better manage their epilepsy
EDEN’s data is available to every stakeholder, provided the patient has consented effectively breaking data silos
we are opening a new era of clinical research driven by patients & democratizing the collection of data& its benefits
Track your epilepsy, answer surveys and access your health data at home or on the go. With EDEN on Embleema’s technology, your health is always at your fingertips.
It’s never been easier to stay on top of your epilepsy. Our user’s time is valuable so we work to make it as quick and easy as possible for them to do what is needed to track and stay on top of their health and wellness.
JACQUELINE FRENCH, MD
Professor of Neurology, NYU Comprehensive Epilepsy Center, New York University, Director Epilepsy Study Consortium, Chief Medical & Innovation Officer, Epilepsy Foundation