Case Study: Pharmaceutical Company reduces clinical trial supply reconciliation time with Clinical Ink SureSource

Maximize Quality, Compliance & Efficiency Via Electronic Drug Accountability

A pharmaceutical company conducting a Phase I study needed a better way to manage clinical drug accountability and supply data, speed access for stakeholders, and reduce paper-based errors in drug accountability, supply, and patient consent. Clinical Ink was brought in to help streamline the process and improve compliance, transparency, and efficiency.

Using Clinical Ink’s SureSource platform, the sponsor deployed eSource tablets and scanning devices to capture source data, drug supply information, and electronic patient consent. The system provided real-time remote access through a web portal and reduced supply reconciliation from more than five hours to 30 minutes, while improving monitoring efficiency and data quality.