Case Study: Top-10 Pharmaceutical Company achieves unified paper/eConsent management and drastic site administrative reductions with Medable's Total Consent

Integrating consent data to reduce administrative burden

A Top-10 Pharmaceutical Company needed to drastically reduce administrative burden on its clinical trial sites and sponsor teams by adopting a single informed consent solution that could handle both paper and electronic consents and populate site IRB, EDC, and internal systems. They selected Medable and its consent product, Total Consent, to meet these requirements.

Medable implemented Total Consent to manage paper and eConsent in one system, standardize consent metadata (e.g., sign date, form title) and automatically route that data to sites’ IRB and EDC systems. The result: participants could choose the consent format that suited them, the sponsor used one centralized consent system, and site personnel reported a dramatic reduction in manual administrative work—saving countless hours and earning high client satisfaction with Medable’s solution.