Almac’s eConsent platform streamlines both electronic and paper-based consent for global clinical trials. It ensures regulatory compliance, enhances participant understanding, and reduces the administrative burden for research teams.
The platform is flexible, supporting both remote and in-person deployment and can be implemented as a standalone module or as part of the Almac Trial Coordinator™ ecosystem for end-to-end workflow efficiency. This unified approach provides sponsors with real time, reliable data and premium services, empowering better decision-making at every stage of the study
