Medidata’s eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. Through the use of multimedia technology, your patients are educated and guided through understanding key elements of a clinical trial.
Whether on-site or remote, eConsent can be used for your clinical study consents, disease registries, and biobanking registries. eConsent provides patients, sites, CROs and sponsors a unified experience for enrollment while delivering additional study analytics to the study team to understand trends and insights from the consenting and reconsenting process.
- Greater Efficiency
- A Unified Approach
- A Better Patient Experience
- Path to Virtual & Hybrid Studies