What is Tilda?
Tilda acts as an AI teammate, working alongside clinical research teams to streamline operations. It integrates with established tools and processes and simplifies trial management for sponsors, sites, and CROs.
The platform offers extensive automation capabilities, resulting in improved data quality, faster timelines, and real-time centralized monitoring. Tilda also offers features like faster site selection and activation, better trial monitoring and quality, automated compliance, and real-time visibility.
Features
- Better data quality and faster timelines: Extensive automation results in demonstrably better data quality and faster timelines.
- Real-time Centralized Monitoring: Access secure, live data instantly for effective trial oversight and decision-making.
- Seamless Regulatory Compliance: Ensure global compliance and maintain inspection readiness with built-in adherence to international guidelines.
- Automated workflows reduce site burden: Eliminate double data entry, boost protocol compliance, and enhance study quality.
- Increase Financial Performance: Boost collection rates, reduce revenue leakage, and improve cash flow.
- Faster site selection and activation: Streamlines the process of identifying and activating appropriate clinical trial sites.
Use Cases
- Automating study management to reduce time and cost.
- Streamlining study setup and maintenance processes.
- Providing real-time data for trial oversight and decision-making.
- Ensuring global compliance and maintaining inspection readiness.
- Eliminating double data entry and boosting protocol compliance at sites.
- Improving cash flow with automated payment tracking and intelligent follow-up systems.
