Medidata eConsent – Empowering Patients Right From The Start

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.

Product Benefits

• Greater Efficiency
• A Unified Approach
• A Better Patient Experience
• Path to Virtual & Hybrid Studies